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H-Lys(Z)-OBzl HCl

    • Product Name H-Lys(Z)-OBzl HCl
    • Alias Bzl-Z-Lys-OH HCl
    • Einecs 259-480-6
    • 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

    207354

    Product Name H-Lys(Z)-OBzl HCl
    Synonyms Nα-benzyloxycarbonyl-L-lysine benzyl ester hydrochloride
    Molecular Formula C21H25ClN2O4
    Molecular Weight 404.89 g/mol
    Appearance White to off-white powder
    Purity Typically ≥98%
    Cas Number 2958-99-2
    Storage Temperature 2-8°C
    Solubility Soluble in DMF, DMSO, and methanol
    Application Peptide synthesis
    Protecting Groups Z (benzyloxycarbonyl) and OBzl (benzyl ester)
    Form Hydrochloride salt
    Smiles C1=CC=C(C=C1)COC(=O)[C@@H](CCCCN)NC(=O)OCC2=CC=CC=C2.Cl

    As an accredited H-Lys(Z)-OBzl HCl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical H-Lys(Z)-OBzl HCl is packaged in a sealed amber glass vial containing 5 grams, labeled with safety information.
    Shipping H-Lys(Z)-OBzl HCl is shipped in tightly sealed containers under cool, dry, and well-ventilated conditions. The package includes appropriate hazard labeling, with necessary documentation to comply with chemical transport regulations. To prevent moisture and light exposure, secondary packaging is often used. Handle with care to avoid spills or contact.
    Storage H-Lys(Z)-OBzl HCl should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place—ideally at 2-8°C (refrigerated). Avoid exposure to strong acids, bases, or oxidizing agents. Ensure the storage area is well-ventilated and accessible only to trained personnel. Proper labeling and away from incompatible substances are essential.
    Application of H-Lys(Z)-OBzl HCl

    Applications of H-Lys(Z)-OBzl HCl in Industrial Manufacturing

    As an experienced chemical raw material manufacturer, we supply H-Lys(Z)-OBzl HCl to high-purity downstream industries. This protected amino acid finds consistent use in controlled chemical synthesis where precision, compliance, and performance integrity are required. Below, we detail verified B2B industrial application fields.

    1. Peptide Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies employ H-Lys(Z)-OBzl HCl as a key protected lysine building block during stepwise peptide chain extension via solution phase or solid phase peptide synthesis (SPPS). Its benzyl and carbobenzyloxy protecting groups ensure selective reaction at desired sites, simplifying deprotection workflows. End users integrate this intermediate into validated GMP-compliant peptide syntheses for injectable and oral drug substances targeting metabolic, tumor, and cardiovascular indications. Quality and traceability must satisfy both local and international regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) relevant amino acid monographs
    • European Pharmacopoeia chapter 5.10 on amino acid derivatives
    • FDA 21 CFR Part 211 for finished pharmaceuticals where applicable

    Typical usage ratio

    • 1.0 – 1.2 molar equivalents per target lysine residue in peptide sequence, adjusted for chain length and batch scale

    Downstream process integration

    • Used at protected lysine coupling steps during SPPS or solution-phase assembly
    • Integration into synthesis workflow after resin loading or prior to amidation/chain extension
    • Deprotection protocols using hydrogenolysis or acidolysis allow specific removal in final steps

    Final product types

    • Generic and innovator peptide APIs (e.g., desmopressin, octreotide, leuprolide)
    • Custom polypeptides for R&D, clinical, and preclinical studies
    • Key intermediates for peptidomimetics

    2. Diagnostic Peptide Manufacturing

    Manufacturers of in-vitro diagnostic reagents and antigen standards use H-Lys(Z)-OBzl HCl during the assembly of synthetic peptides that serve as molecular probes, calibrators, or capture antigens. Its protective groups control site-specific incorporation, thus maximizing selectivity and purity in analytical platforms, including immunoassays and clinical chemistry kits. These peptides ultimately require analytical certificates traceable to ISO and traceability protocols.

    Industry compliance standards

    • ISO 13485 for medical device Quality Management Systems
    • CLSI C62 guidelines for peptide calibrators
    • Relevant FDA 21 CFR Part 820 requirements for diagnostic reagents

    Typical usage ratio

    • 0.8 – 1.1 molar equivalents per diagnostic peptide chain position, depending on sequence complexity

    Downstream process integration

    • Incorporated at precise coupling phases during automated or manual SPPS workflows
    • Deprotected and purified before formulation into diagnostic standards or probe reagents

    Final product types

    • ELISA and CLIA reference peptides
    • Antigen standards for infectious disease assays
    • Analytical grade peptide calibrators

    3. Cosmetic Peptide Ingredient Production

    Producers of cosmetic peptides employ H-Lys(Z)-OBzl HCl when manufacturing short-chain bioactive sequences for premium skincare formulations. The protected derivative enables synthesis of peptides that maintain defined spatial structure, necessary for targeted action in anti-aging, moisturizing, or skin-brightening end products. Cosmetic peptide manufacturing must follow safety, purity, and labeling regulations established by global authorities for dermocosmetics.

    Industry compliance standards

    • Cosmetics Regulation (EC) No. 1223/2009 in the EU
    • ISO 22716:2007 for good manufacturing practices in cosmetics
    • Safety Evaluation of Materials (OECD 431/439 for in vitro skin irritation)

    Typical usage ratio

    • 1.0 equivalent per modified lysine in cosmetic peptide backbone, fine-tuned by manufacturing lot size and sequence sensitivity

    Downstream process integration

    • Added to automated peptide synthesizer or solution reactors at lysine coupling stage
    • Deprotection performed after primary sequence assembly and before final purification

    Final product types

    • Palmitoyl oligopeptide and tripeptide actives for serums
    • Cosmetic peptides for anti-wrinkle creams
    • Active ingredients in skin repair gels

    4. Research-Grade Peptide Library Synthesis

    Academic and contract research organizations routinely consume H-Lys(Z)-OBzl HCl during combinatorial library synthesis. This derivative supports rapid, protected coupling cycles needed for generating large arrays of peptides with high positional selectivity. End users rely on its consistent quality for reproducible parallel synthesis, often on automated robotic platforms, facilitating hit identification with site-specific modification.

    Industry compliance standards

    • National Institutes of Health (NIH) chemical safety and handling guidelines
    • OECD Principles of Good Laboratory Practice for non-clinical labs
    • GLP requirements for academic and CRO research facilities

    Typical usage ratio

    • 0.95 – 1.05 equivalents per lysine site per synthesis cycle, customizable by peptide length and library diversity

    Downstream process integration

    • Programmed addition at each lysine position during automated or semi-automated peptide synthesis
    • Deprotection executed post-assembly for global or segmental libraries

    Final product types

    • Synthetic peptide libraries for screening
    • Bioassay probe libraries
    • Site-mutated peptide sets

    5. Specialty Bioconjugate Synthesis

    Producers involved in diagnostics and therapeutics leverage H-Lys(Z)-OBzl HCl for specialty synthesis of peptides requiring site-specific bioconjugation. The protective groups on lysine permit orthogonal modification, critical for downstream coupling of fluorophores, drugs, or affinity tags while avoiding cross-reactivity at undesired positions. This yields high-value bioconjugates for targeted imaging, delivery, or immunoassay detection.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management Systems in chemical manufacturing
    • EMA Guidelines on the Chemistry of Bioconjugates
    • REACH Regulation (EC) No. 1907/2006 for safe chemical handling

    Typical usage ratio

    • 1.0 equivalent at protected lysine residue, with adjustment for multi-site or single-site conjugation design

    Downstream process integration

    • Integrated into bioconjugation workflows at peptide assembly step
    • Deprotection scheduled prior to selective labeling with imaging or affinity moieties

    Final product types

    • Peptide-fluorophore conjugates for flow cytometry and imaging
    • Drug-peptide conjugates for targeted delivery
    • Affinity-tagged peptides for immunoprecipitation kits
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    Certification & Compliance
    More Introduction

    H-Lys(Z)-OBzl HCl: Direct Insights from Our Production Floor

    Bringing Chemistry to Life with H-Lys(Z)-OBzl HCl

    Years of work in peptide synthesis labs have proven that the choice of protected lysine derivatives can make or break production efficiency and product quality. Our team stands daily among flasks and reactors, so we understand the challenges. H-Lys(Z)-OBzl HCl has found favor with researchers and scale-up chemists because it enables solid and solution-phase approaches without introducing unwelcome side reactions. Our facility focuses on this compound because the market consistently asks for dependable, clean, and well-characterized batches, especially when synthesizing longer peptides and complex therapeutic candidates.

    Model and Specifications: Proven Methods in Action

    We manufacture H-Lys(Z)-OBzl HCl in accordance with time-tested procedures, starting with L-lysine and applying rigorous control from hydrogenation to finished purification. Our standard batch size typically supports demands ranging from small pilot projects to full-scale biotech production. Over the years, we’ve found that controlling for chloride content and residual solvents improves downstream reactions. Each lot is monitored for optical purity, moisture, and particle size because even minor variations create noticeable headaches during coupling. Our analytical methods have evolved alongside industry requirements, so we validate the identity using NMR, HPLC, and MS on every release—because someone will check, and cutting corners only complicates things later.

    Molecular formula: C21H25ClN2O4. Content per batch always exceeds 98%, as verified by HPLC. Residual solvent and heavy metals sit well below established pharmacopeial limits. Moisture content is measured by Karl Fischer titration, never exceeding 0.5%, because excess water disrupts the activation of carboxyl groups in the Fmoc or Boc-based chemistries our customers prefer.

    Why Synthesize with H-Lys(Z)-OBzl HCl?

    We’ve rolled out drums of Fmoc-Lys(Boc)-OH, Boc-Lys(Z)-OH, and others over the decades, but many clients return to H-Lys(Z)-OBzl HCl when selectivity matters or cost savings are critical. Its strong-point lies in the unique pairing of the benzyloxycarbonyl (Z) group and the benzyl ester (OBzl) cap, both removable under hydrogenolysis—one step, two protections gone. This saves precious time compared to the sequential deprotection most alternatives need. Our experience shows reduced byproduct formation in peptide couplings and fewer impurities in the crude final product, which translates to better yields and less time lost during final purification.

    We routinely witness researchers switching to H-Lys(Z)-OBzl HCl for longer, more hydrophobic peptides where side reactions with alternative protecting groups—such as acidolysis-labile Boc—compromise yields. It shows particular value in the assembly of protected peptide fragments prior to final global deprotection. Simultaneous removal of Z and OBzl in one hydrogenation step encourages rapid process development, especially in milligram-to-gram scale batches.

    Comparing H-Lys(Z)-OBzl HCl to Other Derivatives

    The market is saturated with lysine derivatives: Fmoc-Lys(Boc)-OH works well for automated solid-phase synthesis, while Boc-protected lysines dominate in solution chemistry. H-Lys(Z)-OBzl HCl stands out because its dual protection staves off both acid- and base-catalyzed cleavage, so intermediate handling proves less risky than with labilized protecting groups. We see strong customer preference for this product in synthesis pipelines where sequential acid/base steps cannot be avoided, because Z and OBzl protections endure routine deprotection conditions.

    Several alternatives, like Fmoc-Lys(Boc)-OH or Lys(Z)-OH, come with their own drawbacks. The Fmoc group, widely used for solid-phase synthesis, easily falls off with moderate bases—making it less suitable for complex fragment condensation steps. Boc-protection, popular for its ease of removal under TFA, can break down during some condensation or cyclization conditions, introducing ugly side-products. Our customers who run hydrogenolysis at scale routinely complain about extra steps when using single-protected lysines, so H-Lys(Z)-OBzl HCl puts them back on track with more efficient workflows and consistent product clean-up.

    Beyond the Chemistry: What Our Factory Sees

    As chemists, we acknowledge that minor differences in protecting group stability appear trivial on paper, but these differences burn through budgets during multi-kilo synthesis or GMP campaigns. Our technical team fields inquiries about compatibility of H-Lys(Z)-OBzl HCl with various peptide linkage strategies. In actual process runs, it has proven suitable in carbodiimide-mediated couplings, HATU- or PyBOP-assisted strategies, and even enzymatic transformations. Early batches, a decade ago, displayed variable moisture content, which complicated scale-up and led to batch fails for one major client. We learned quickly to dry under vacuum and fill under nitrogen to preserve integrity, which has cut product complaints to nearly zero.

    Our process development chemists watch for trends in global regulations. H-Lys(Z)-OBzl HCl is made without phthalate plasticizers or solvents attracting regulatory scrutiny. We make sure to keep impurities under close watch—benzyl chloride, toluene, and other benzyl reagents can sneak into the workflow, so regular GC and LC checks are a non-negotiable part of our workflow.

    Supporting the Front Lines of Research

    We see first-hand how time delays in critical peptide building blocks grind pharma campaigns to a crawl. Peptide synthesis groups, custom manufacturing organizations, and academic teams all rely on reliable shipments of H-Lys(Z)-OBzl HCl. Poor solubility or inconsistent packing density used to halt reactions at scale, so we invested in micronization and controlled crystallization to produce material that dissolves consistently and avoids troublesome aggregates.

    Often, early process R&D struggles with inter-batch variability. By carefully tracking impurities—such as incompletely removed hydrogenolysis catalysts or oxidative by-products—we help avoid downstream equipment fouling and chromatogram headaches. Providing comprehensive analytical packages cuts down on the back-and-forth between labs. Quality issues crop up immediately during resin loading for solid-phase synthesis, so our team monitors lot-to-lot consistency at this critical point. Few things frustrate a production chemist more than blaming failed couplings on raw materials, so we take it personally to make sure our H-Lys(Z)-OBzl HCl doesn’t create slowdowns.

    Global Trends and Ongoing Challenges

    Increasing regulatory and customer focus on traceability, impurity profiling, and environmentally responsible production force us to adapt faster than ever. H-Lys(Z)-OBzl HCl, thanks to its robust benzyl-based protections, continues to prove itself in both R&D and GMP manufacturing because process changes can be implemented without major revalidation efforts. Global competition in peptide active ingredients has not slowed demand—instead, it’s made reliable, reproducible supply chains even more necessary.

    Raw material availability, especially for benzyl chloride and related derivatives, formerly put strain on production costs. Improvements in supplier monitoring and logistics long ago taught us the pitfalls of single-source dependencies. This means every batch receives not just purity and performance checks but also routine screenings for key trace chemicals, so we sidestep process upsets that can gum up full downstream campaigns and lead to production stops.

    Our Perspective on Safety and Handling

    Every technician in our facility goes through regular training on handling protected amino acids because many of these materials, especially those with benzyl groups, demand careful control during hydrogenolysis. Overexposure to hydrogen, traces of Pd/C, or incomplete gas removal cause issues, so years of experience help us guide users on best practices: degas thoroughly, run hydrogenations to completion, filter out catalyst residues, and monitor for byproduct amines. Adhering to rigorous in-house handling protocols has dramatically reduced incident rates and customer complaints about post-take-off purity or contamination.

    Many customers operate open-vessel reactors or older hydrogenation setups. To address this, we normalize strict monitoring of pressure and temperature, and recommend filtration under inert gas to minimize benzylamine carryover. Such steps, though simple, improve the safety and outcome of every hydrogenolysis, especially for those not blessed with all the latest reactor tech.

    Differentiation in the Field: Listening to Chemists’ Gripes

    Too many times, chemists come to us complaining about inconsistent yields or peculiar byproducts from less rigorously produced amino acid derivatives. Our own operations have seen cases where materials sourced from loosely monitored sources, or repacked by resellers, introduce micro-contaminants that realign the entire impurity profile of a peptide run. By controlling every step—in-house chemical synthesis, purification, packaging in humidity-controlled environments, and prompt delivery—our focus remains on providing a tool, not a source of unexplained variance.

    Customers share frustration about “mystery peaks” in chromatograms—unlabeled, leftover derivatives, or tars resulting from incomplete benzyl group cleavage. To mitigate this we document catalyst loading, hydrogen pressure, and filtration specifics for each batch, then pass that know-how to users. In our experience, competing products featuring only a single protective group tend to fall short when facing diverse chemistries, requiring labor-intensive extra purification, and costing more in the long run.

    User-Centric Development: Honest Feedback Shapes Our Supply

    Feedback loops drive change in specialty chemical manufacturing. Our product development chemists don’t just sit with spreadsheets—they pore over results from our clients’ syntheses, whether those results sing or complain. Over the last few years, users shifting from Boc- or Fmoc-protected lysines to H-Lys(Z)-OBzl HCl often cite reduced step count and cleaner spectra as priorities. Their honesty fuels improvements in drying methods, powder flowability, and shelf-life stability. Early feedback highlighted issues with aggregation on storage, so we adjusted crystallization practices and improved packaging, sparing many downstream headaches and adding shelf-life stability as a byword in our internal checklists.

    Economic Pressures and Value Assessment

    Market volatility, raw material fluctuations, and escalating regulatory requirements all challenge our pricing models. H-Lys(Z)-OBzl HCl still offers more process flexibility than most alternatives, saving steps in large-scale peptide syntheses and cutting secondary deprotection runs. From our vantage point, value comes not in cutting quality for a lower sticker price, but in minimizing waste, avoiding resynthesis, and sending out shipments that perform to expectation every single time. Our cost calculators build in what happens at the bench: fewer failed runs, faster scale-ups, fewer purification headaches.

    Continuous Improvement: Leaning on Science, Not Hype

    As new synthetic methodologies emerge—flow chemistry, novel coupling agents, greener solvents—H-Lys(Z)-OBzl HCl continues to find its place due to robust, well-understood chemistry. Our pipeline includes regular reviews of coupling yields across downstream partners. Real-world feedback, not glossy marketing, drives updates to our standard operating procedures. We support open communication with R&D teams because successful chemistry relies on real transparency; only then can users trust the materials they work with—and that trust, once lost, never returns easily.

    Conclusion: A Manufacturer’s View on Doing It Right

    Much has changed since we first stood up our first H-Lys(Z)-OBzl HCl line, but the basic truths of chemical manufacturing remain. Paying attention to the details—purity, stability, and effective communication—translates to better research outcomes, fewer late-night troubleshooting sessions, and chemicals you can rely on batch after batch. Our product stands as a testament to those lessons. We don’t treat H-Lys(Z)-OBzl HCl as just another SKU; we treat it as a vital tool supporting advances in science, because that’s exactly what it is.