Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Z-Leu-OSu

    • Product Name Z-Leu-OSu
    • Alias N-Succinimidyl N-benzyloxycarbonyl-L-leucinate
    • Einecs 252-896-8
    • 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
    VTB
    Specifications

    HS Code

    507974

    Product Name Z-Leu-OSu
    Chemical Name N-CBZ-L-leucine N-hydroxysuccinimide ester
    Molecular Formula C19H24N2O6
    Cas Number 1993-49-1
    Appearance White to off-white powder
    Solubility Soluble in DMSO, DMF, and chloroform
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Application Peptide synthesis coupling reagent

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

    Packing & Storage
    Packing Z-Leu-OSu is supplied in a 1 gram amber glass vial, tightly sealed, labeled with product name, CAS, and lot number.
    Shipping Z-Leu-OSu is shipped in tightly sealed containers, protected from moisture and light. Packages are clearly labeled and compliant with chemical transportation regulations. During transit, temperature is kept at room temperature, unless specified otherwise. All shipments include necessary documentation such as Safety Data Sheets (SDS) for safe handling and regulatory compliance.
    Storage Z-Leu-OSu should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at -20°C. Avoid excessive heat and humidity to prevent degradation. Ensure the storage area is well-ventilated and chemicals are clearly labeled. Follow all safety guidelines for handling reactive organic compounds.
    Application of Z-Leu-OSu

    Applications of Z-Leu-OSu in Industrial Manufacturing

    Z-Leu-OSu (N-Carbobenzyloxy-L-leucine N-succinimidyl ester) is a specialized N-protected amino acid active ester, widely utilized in peptide synthesis due to its selectivity, stability, and compatibility with stringent quality standards. As a core coupling reagent, it finds application in pharmaceutical, biochemical, and life sciences manufacturing workflows where precision and batch-to-batch reproducibility are non-negotiable. Below, we present the principal industrial segments and the corresponding technical application details.

    1. Active Pharmaceutical Ingredient (API) Peptide Synthesis

    Pharmaceutical CMO/CDMOs and large-scale API producers rely on Z-Leu-OSu during solid phase and solution phase peptide synthesis, particularly for incorporating protected leucine residues in complex peptide chains and cyclic peptides. Stringent regulatory controls ensure control of residual reagents and byproducts throughout the process, especially during GMP-controlled lot production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs (peptide APIs)
    • US FDA cGMP 21 CFR Part 210/211
    • Chinese Pharmacopoeia peptide quality standards

    Typical usage ratio

    • Range: 1.0–1.5 molar equivalents per N-terminal amine; fine-tuned according to resin loading and active ester reactivity. Higher ratios applied in sequences requiring exhaustive coupling to address steric hindrance.

    Downstream process integration

    • Pre-activation step in solid and solution phase peptide elongation (Fmoc/Boc strategies); added after initial amino acid deprotection before N-terminal coupling.

    Final product types

    • Therapeutic peptides (injectable APIs)
    • Peptide-based diagnostic reagents
    • Generic peptide drug substances for formulation
    • Clinical-grade peptide intermediates

    2. Cosmetic Peptide Ingredient Manufacturing

    Manufacturers of functional cosmetic peptides utilize Z-Leu-OSu for site-selective introduction of protected leucine in bioactive motifs such as anti-wrinkle or skin-brightening peptides. Compliance with cosmetics regulations and adulterant control form the backbone of manufacturing quality, with documentation for absence of residual reactive intermediates to support safety assessments.

    Industry compliance standards

    • EU Cosmetic Regulation (EC) No 1223/2009
    • ISO 22716: Cosmetics — Good Manufacturing Practices (GMP)
    • CTFA/PCPC Ingredient Labelling and Purity Guidelines
    • China Cosmetic Supervision and Administration Regulation (CSAR) for peptide raw materials

    Typical usage ratio

    • 0.9–1.2 equivalents per coupling step, as dictated by the complexity of the peptide and side chain protection scheme. Adjusted to minimize excess reagent and facilitate purification.

    Downstream process integration

    • Applied directly after N-terminal deprotection during the synthesis of short bioactive peptides and cosmetic peptide libraries, typically at small-to-medium batch scale.

    Final product types

    • Anti-aging peptide actives (e.g., pentapeptide-4 derivatives)
    • Whitening peptide prototypes for cream/serum applications
    • Synthetic tripeptides for hair care actives
    • Biofunctional peptide powder concentrates

    3. Research-Grade Custom Peptide Synthesis

    Biotechnology companies and laboratory-scale peptide manufacturers deploy the active ester for rapid, small-batch synthesis of modified peptides. Focus lies on minimizing side-reactions and maximizing sequence fidelity, especially for analytical standards, epitope mapping, and academic research peptides where reproducibility and documentation are crucial for scientific validation and regulatory submissions.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for laboratory suppliers
    • GLP (Good Laboratory Practice) as defined by OECD for research-grade reagents
    • Internal QA/QC protocols for peptide traceability
    • Material Safety Data Sheet (MSDS) requirements for shipped chemicals

    Typical usage ratio

    • 0.95–1.1 molar equivalents, typically calibrated to maximize coupling efficiency and lower purification burden on the preparative HPLC system

    Downstream process integration

    • Used in N-terminal or side-chain functionalization steps for laboratory-scale and pilot batches, integrated during manual or automated synthesis cycles

    Final product types

    • Custom peptide libraries for drug screening
    • Epitope mapping standards
    • Protease substrate peptides
    • Chemically labeled peptide tracers for academic studies

    4. Enzyme Substrate and Diagnostic Kit Production

    Diagnostic manufacturers incorporate Z-Leu-OSu to develop synthetic enzyme substrates for use in colorimetric, fluorometric, and luminescent assays. The raw material enables the introduction of specific amino acid sequences to enhance substrate selectivity and kinetic properties, critical for use in regulated medical device workflows and in vitro diagnostics where consistent batch quality is mandatory for reliable test kit performance.

    Industry compliance standards

    • ISO 13485: Medical Devices — Quality Management System
    • FDA 21 CFR 820 Quality System Regulation for Medical Devices
    • IVDR (EU) 2017/746 Regulation for In Vitro Diagnostic Medical Devices
    • OECD principles for diagnostic reagent labeling and quality

    Typical usage ratio

    • 1.0–1.3 equivalents per synthetic step, adjusted based on enzyme substrate turnover number and assay format to optimize substrate performance

    Downstream process integration

    • Engaged at the step introducing leucine residues into peptide-based substrate sequences in solid phase assembly prior to cleavage and final purification

    Final product types

    • Chromogenic peptide substrates for protease assays
    • Fluorogenic probes for clinical diagnostics
    • Chemiluminescent enzymatic substrates
    • Ready-to-use assay kit components
    Free Quote

    Competitive Z-Leu-OSu prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Z-Leu-OSu in Peptide Synthesis: A Manufacturer’s Perspective

    The years invested in producing and refining Z-Leu-OSu have taught us a few straightforward truths about peptide coupling agents. Z-Leu-OSu, the N-succinimidyl ester of carbobenzoxy-protected leucine, has earned its place in our catalog because it strikes the balance between reactivity and selectivity that experienced chemists count on. In peptide research and development labs, we've noticed a steady increase in the use of activated esters such as this one. The choice isn't made lightly—researchers demand precision in every coupling reaction. Z-Leu-OSu provides that, while reducing unwanted byproducts and streamlining post-reaction workups. Years of feedback from peptide chemists has shaped the product into what it is today.

    Why We Focus on Z-Leu-OSu

    Developing and manufacturing Z-Leu-OSu is more than an exercise in organic synthesis. The process begins with stringent raw material selection—impurities from L-leucine or carbobenzoxy chloride can create headaches down the line, causing low yields and troublesome purification steps. Early on, we set diligent controls on every input. We rely on careful esterification and purification to get crystalline Z-Leu-OSu with consistent characteristics. The final product must provide sharp melting points and meet strict NMR and HPLC criteria. Downstream users expect every batch to dissolve easily and react as predicted.

    This product’s primary role centers on peptide coupling, and peptide chemists expect more than commodity-grade raw materials. Coupling L-leucine residues, especially toward the N-terminus, can present challenges from steric hindrance or racemization. Z-Leu-OSu’s design—anchored by the carbobenzoxy group and the active N-hydroxysuccinimide leaving group—minimizes these issues in practice. We have processed thousands of batches and taken laboratory feedback seriously: users see lower epimerization and good reproducibility across scale—from milligrams to kilograms.

    Understanding Our Manufacturing Rigor

    The story of Z-Leu-OSu doesn’t begin or end at the flask. Running the process brings challenges that teach lessons about moisture control, temperature regulation, and patience with crystallization. During summer, increased ambient humidity tests our solvent handling; scrambled steps here can balloon impurity profiles, making additional purification necessary. Over the years, process tweaks have lowered contamination risk. Wet assays, high-resolution chromatography, and precise drying control ensure that what leaves our facility performs predictably in downstream applications.

    Some competing products flood the market with variable quality, a problem evident in peak broadening on HPLC or sluggish coupling reactions. We never stop batch-testing for unwanted byproducts—N-hydroxysuccinimide dimer, acid hydrolysis fragments, oxidized Z-Leu—since they eat away at overall coupling yield and complicate final peptide isolation. Every time a batch comes off our production line, it goes through panel review before shipment.

    Comparison to Other Coupling Agents

    Peptide chemists juggle a long list of coupling options, but each comes with trade-offs. Active esters of leucine range from the p-nitrophenyl derivative to mixed anhydrides, each with quirks unique to their chemistry. Z-Leu-OSu, in our hands, offers a sweet spot: sufficient reactivity without the overzealous background acylation seen with pure acid chlorides. Unlike DCC or HATU-mediated methods, it sidesteps toxic byproducts or urea residues that complicate clean-up and regulatory documentation. The N-succinimidyl moiety stands out for ease of handling—it’s stable for storage, non-hygroscopic with the right drying, and amenable to scale-up.

    Clients new to peptide synthesis sometimes ask about the differences. We’ve seen consistent results—higher yields, simpler purifications, and lower process waste—compared to cost-cutting alternatives. Peptide projects benefit from the reliability, especially in solid-phase work or segments prone to racemization. Our R&D department runs head-to-head comparisons regularly to keep any drift in quality in check; when irregularities sneak in, they become apparent long before shipment.

    Specifications Built on Feedback and Experience

    Years ago, our product line offered Z-Leu-OSu in different purity ranges and particle sizes. The laboratories using these reagents spoke clearly: they wanted high purity, reliable reactivity, and solid documentation backing every lot. We responded by tightening our final purification to keep purity above 99%, as determined by both HPLC and NMR. Fine control over particle size distribution made dissolution in common solvents—DMF, DCM, acetonitrile—quick and uniform, removing one more variable from complex synthetic planning.

    In a push for full transparency, every batch comes with full analytical data. Instead of generic statements, our documentation details chromatographic purity, water content, and precise melting points. No two processes run in perfect isolation, and sharing this level of detail lets users troubleshoot much more quickly. We update our QC protocols regularly in response to user feedback and to stay current with evolving analytical technology.

    It’s easy to ship powder with a label attached. Supplying what labs genuinely need day after day takes longer. Our batches run from pilot scale to industrial quantities on demand, helped by staggered production lines that can adapt to urgent orders. Cold-chain handling and chemical stabilization guarantee performance months or even years after packaging.

    Daily Laboratory Value and Project Impact

    Those who run solid-phase and solution-phase peptide syntheses know firsthand where bottlenecks begin. Installation of leucine residues is a common pain point, especially when building hydrophobic segments. Z-Leu-OSu makes clean couplings more repeatable, so peptide bonds form fully with minimum side reactions. This property translates to faster development timelines and less troubleshooting—a concern for all manufacturers as much as for peptide research labs.

    Over the years, many researchers have come to us with the same story: an unreliable coupling step stalling entire projects. Substandard active esters can introduce hidden impurities or incomplete reactions, which cost time and resources to resolve. Switching to consistently high-quality Z-Leu-OSu has allowed faster progress and easier downstream purification for a range of projects, from early academic research to later-stage pharma development. Analytical groups often comment on the clarity of their HPLC and LC-MS data after making the switch.

    Partnering with customers at the technical level matters just as much as selling the material. We encourage open communication, and routinely field questions about solvent choice, coupling conditions, and impurity handling. The most productive labs give us feedback on how Z-Leu-OSu holds up under challenging conditions and which protocols deliver the cleanest results. This two-way learning loop lets us keep improving—right down to packaging material upgrades and custom batch sizing.

    Supporting the Push for Cleaner Chemistry

    The drive toward greener, safer chemistry has pushed every manufacturer to rethink their processes. We took early steps to minimize chlorinated waste and look for safer alternatives in our Z-Leu-OSu production. Excess solvents are collected and recycled within the plant; waste streams pass through neutralization and filtration to meet environmental rules. Fewer hazardous reagents reduce risk to operators, resulting in a safer workplace and cleaner finished goods.

    We also see an increased demand for documentation covering origin, impurity profiling, and transportation. Project managers want more than an invoice—they want to know their building blocks are produced under responsible, trackable conditions. We routinely provide origin traceability, batch numbers, and detailed MSDS breakdowns. As regulatory bodies increase their scrutiny, especially in pharmaceutical projects, suppliers need to step up with products that don’t add headaches at the compliance review stage.

    Responsible sourcing and detailed analytics benefit our customers. Peptide synthesis moves toward cGMP and stricter safety rules; every reagent in the chain must meet higher bars. Since contamination or impurity transfer can’t always be resolved in the final purification, clean starting materials save much more time and money than some users initially expect.

    Packaging, Storage, and Customer Service Insights

    Observing the changes in how chemists store and use Z-Leu-OSu has shaped our approach to packaging and distribution. Exposure to light, heat, or trace moisture gradually degrades active esters—that’s a lesson lab managers learn quickly. We switched to amber vials and airtight containers, evacuated bags, and small-lot packaging so end users avoid multiple freeze-thaw cycles and excessive transfer losses. Larger volumes for industrial sites come in secondary containment with built-in desiccants.

    Our customer support team keeps logbooks. Calls from the field reveal where problems arise—from discolored product due to sunlight to caking in high-humidity environments. Feedback loops feed into continuous improvements. Our current packaging line builds off this accumulated experience, reducing both visible degradation and unseen micro-contamination between manufacturing and benchwork.

    Every laboratory sets up its own communication protocols, documentation needs, and reagent tracking. Our support team fields requests for custom labeling, barcoding, and electronic documentation transfer to support inventory tracking. We work closely with both academic purchasing offices and industrial scale-up teams to anticipate customs queries and avoid clearance delays. This level of attention reflects years of direct interactions and a shared goal: steady, predictable projects with no last-minute reagent changes.

    Practical Considerations for Regular Users

    In daily routines, Z-Leu-OSu stands out for how it simplifies coupling steps and cuts troubleshooting time. Chemical manufacturers and bench chemists alike find value in its long shelf-life, which holds steady under standard low-temperature storage. We advise storage below ambient temperature, protected from light, and capped airtight. Immediate use after dispensing is ideal, but if extended storage is needed, users report minimal decomposition or handling difficulties.

    Direct communication with synthesis teams across geographic regions has revealed practical differences in usage. Some regions see more humidity; others run older gloveboxes or open-bench procedures. Norms in reagent handling change with experience. We listen carefully to preferences in solvent selection and coupling conditions, noting which operate best: common choices include DMF or DCM as solvents, with mild bases to aid dissolution and minimize racemization. No one protocol fits every lab, but feedback points to a set of robust, predictable practices that reduce troubleshooting and reagent waste.

    Quality lab work depends on the smallest details: uniform weighing, rapid mixing, and complete dissolution. Z-Leu-OSu’s stability and ease of handling free up valuable bench time for more critical tasks. Researchers regularly share time-saving tricks with us: powder pre-aliquoting into light-protected tubes, rapid dissolution in pre-chilled solvent, quick workup for cleaner crude peptides. We keep collecting and relaying these process insights to help improve outcomes across the sector.

    Responding to the Changing Landscape in Peptide Research

    The past decade has seen peptide research move from academic curiosity to the core of many drug discovery efforts. New therapeutic peptides, diagnostics, and labeling projects drive greater demand for building blocks like Z-Leu-OSu that deliver clean reactions and easy purification. Increasingly complex peptide sequences put new stress on every coupling step. As chemists push boundaries in length and complexity, they look for reliable reagents to maximize yields and minimize rework.

    We watch closely how project timelines and batch sizes have changed. Pilot-scale batches may need only grams for a high-profile effort; scale-up teams sometimes require kilograms on short notice for early clinical projects. Our manufacturing system adapted over time, flexing between small custom runs and large, validated batches without letting quality slip. The biggest challenge isn't making a product once—it's producing hundreds or thousands of batches without introducing changes that catch users off guard.

    As clinical and diagnostic peptides surge forward, regulatory expectations rise. Our documentation covers raw material origin, trace levels of regulated impurities, and detailed transport categorization. Project managers in large pharma and small biotech firms now check for these details. Over time, we’ve built relationships founded on clear technical exchanges, timely communication, and the ability to solve unexpected challenges in real time.

    Industry Trends and Forward-Thinking Solutions

    The future of peptide synthesis will bring higher standards for every input. As automation and miniaturized synthesis platforms move to the fore, reagent quality no longer sits in the background. Automated synthesizers magnify the impact of minor reagent impurities or batch-to-batch variability. Our team collaborates with equipment manufacturers and R&D labs alike to troubleshoot bottlenecks—from resin compatibility to optimal coupling conditions with Z-Leu-OSu.

    Our development focuses on reducing environmental impact and boosting reproducibility. New purification steps minimize waste and energy use. Supply chain audits keep counterfeit or off-specification raw materials out. We maintain a close eye on international trends—tightened regulatory rules, changing pharmaceutical demands, and evolving best practices—in order to keep updating our materials and protocols.

    The community of peptide chemists is a resilient, innovative group. We find satisfaction in supporting their evolving work with consistent, clean, reliable Z-Leu-OSu. Between conversations with regular users and targeted R&D investment, we look for issues before they become project risks. The focus stays on actionable process insights, direct technical support, and honest sharing of best practices. This approach has made our Z-Leu-OSu a mainstay in labs that value clear outcomes, rapid troubleshooting, and the freedom to innovate with confidence.

    Conclusion: Trusted Building Block for Tomorrow’s Discoveries

    Our experience manufacturing Z-Leu-OSu for years has shown that reliability, deep product knowledge, and open communication matter most. Whether supporting early research or scaled-up production, these values shape every step. As peptide science advances and demands sharper, cleaner building blocks, we remain ready to adapt alongside our partners—in the factory, the laboratory, and in the field. The lessons learned from years of production help strengthen Z-Leu-OSu for today’s chemists and tomorrow’s breakthroughs.