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Boc-L-lysine

    • Product Name Boc-L-lysine
    • Alias Nα-Boc-L-lysine
    • Einecs 252-910-1
    • 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

    388006

    product_name Boc-L-lysine
    chemical_formula C11H22N2O4
    CAS_number 13734-41-3
    appearance White to off-white powder
    melting_point 98-103°C
    solubility Soluble in water and polar organic solvents
    purity Typically ≥98%
    storage_temperature 2-8°C
    protecting_group Boc (tert-butyloxycarbonyl)
    optical_rotation [α]D +15° to +18° (c=1, H2O)
    synonyms Nα-Boc-L-lysine
    IUPAC_name (2S)-2-[(tert-butoxycarbonyl)amino]-6-aminohexanoic acid
    pKa 2.2 (COOH), 10.5 (NH2)

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

    Packing & Storage
    Packing Boc-L-lysine is packaged in a 25g amber glass bottle, sealed with a plastic cap, and labeled with product and safety information.
    Shipping Boc-L-lysine is shipped in tightly sealed containers under cool, dry conditions to prevent moisture and contamination. The packaging complies with chemical safety standards and includes appropriate labeling for identification and hazard information. During transit, the chemical is protected from heat, direct sunlight, and incompatible substances to maintain product integrity.
    Storage Boc-L-lysine should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry place, preferably at 2–8°C (refrigerator temperature). Avoid exposure to air and strong oxidizing agents. Proper storage ensures the stability of the Boc protecting group and prevents degradation or contamination of the amino acid derivative.
    Application of Boc-L-lysine

    Applications of Boc-L-lysine in Industrial Manufacturing

    Boc-L-lysine serves as a critical protected amino acid intermediate, playing a central role in advanced peptide synthesis processes for pharmaceutical, biotechnology, and chemical sectors. As a direct manufacturer, we supply Boc-L-lysine tailored for industrial-scale applications with a focus on stringent compliance, process optimization, and consistent integration into downstream processes.

    1. Active Pharmaceutical Ingredient (API) Peptide Synthesis

    Pharmaceutical companies employ Boc-L-lysine extensively as a protected lysine residue during stepwise solid-phase peptide synthesis (SPPS) and solution-phase approaches. Its use simplifies sequence assembly while preventing undesired side reactions at the ε-amino group. Within multi-kilogram GMP batch manufacturing, precise control of Boc deprotection and couplings ensures efficient assembly of therapeutic peptide APIs, including modern oligopeptides, peptide hormones, and analogues for regulatory submission and global market release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <1790> and EP 2.9.43 for peptide-related substances and quality attributes
    • US FDA 21 CFR Part 211 for manufacturing controls
    • Current Good Manufacturing Practice (cGMP) certification audit requirements

    Typical usage ratio

    • 0.8–1.2 molar equivalents per lysine position within target peptide sequence
    • Adjustment based on resin substitution rate and peptide chain length

    Downstream process integration

    • Applied during stepwise assembly on resin or in solution
    • Boc deprotection performed with TFA prior to the final deprotection and cleavage
    • Excess removed during intermediate wash cycles and final purification

    Final product types

    • Therapeutic oligopeptide APIs for injection
    • Peptide hormone APIs such as vasopressin analogs
    • Clinical-stage investigational peptide drugs

    2. Diagnostic Peptide Synthesis for In Vitro Kits

    Manufacturers of diagnostic test kits utilize Boc-L-lysine for controlled assembly of functionalized peptides required in immunoassays, biosensors, and ELISA diagnostics. Its role in protecting lysine groups allows selective incorporation of labeled residues and conjugation sites. High-purity Boc-L-lysine ensures batch-to-batch consistency and regulatory compliance during bulk manufacture of critical diagnostic reagents used globally in clinical and research laboratories.

    Industry compliance standards

    • ISO 13485 Medical device and reagent quality management
    • EU IVDR Regulation (2017/746) for in vitro diagnostic use
    • CLSI GP42-A6 for quality control in IVD peptide synthesis
    • Restriction of Hazardous Substances (RoHS) for kit components

    Typical usage ratio

    • 1.0 equivalent per desired protected lysine residue
    • Adjusted based on sequence complexity and labeling positions

    Downstream process integration

    • Introduced during initial peptide elongation steps
    • Selective Boc removal allows for site-directed labeling
    • Purified peptide integrated into diagnostic assay assembly lines

    Final product types

    • Synthetic peptide antigens for ELISA plates
    • Biosensor capture probes
    • Labeled reference peptides for quantitative immunoassays

    3. Biotech Research Reagents Manufacturing

    Biotechnology reagent suppliers rely on Boc-L-lysine to produce custom peptides for academic and industrial R&D. The protection of lysine’s side chain amine enables controlled incorporation into complex peptide libraries, mapping tools, and molecular probes. Quality control is maintained through stringent in-process analytics, supporting global supply to research institutions and contract research organizations.

    Industry compliance standards

    • ISO 9001 quality management systems for reagent manufacture
    • REACH Registration where applicable for export into EEA
    • Material traceability and Certificate of Analysis (COA) requirements
    • Applicable Material Safety Data Sheet (MSDS) documentation for handling

    Typical usage ratio

    • 0.85–1.15 equivalents per protected lysine depending on combinatorial synthesis scale
    • Adjusted for manual or automated synthesis platforms

    Downstream process integration

    • Initiated during synthesis on solid-phase or in liquid-phase batch reactions
    • Boc group removed when selective side-chain deprotection is required
    • Large-scale purification by HPLC, lyophilization, and packaging for research sales

    Final product types

    • Peptide libraries for screening campaigns
    • Protein interaction mapping tools
    • High-purity research-grade peptides

    4. Cosmetic Peptide Raw Material Manufacturing

    Manufacturers supplying finished cosmetic peptides for formulations such as anti-aging creams, serums, and specialty cosmeceuticals leverage Boc-L-lysine as a key protected amino acid. Its use facilitates clean stepwise assembly of functional peptides with lysine-dependent cosmetic activity. Our material meets the quality and impurity thresholds required for downstream skin-contact formulations under international cosmetic regulations.

    Industry compliance standards

    • ISO 22716:2007 Cosmetics — Good Manufacturing Practices
    • Cosmetic Regulation (EC) No 1223/2009 compliance for EU market
    • IFRA ingredient guidelines for safe peptide use
    • Relevant local regulatory listing as cosmetic ingredient

    Typical usage ratio

    • 0.9–1.1 equivalents per lysine in target cosmetic peptide sequence
    • Ratio tailored based on required sequence length and lysine-rich motifs

    Downstream process integration

    • Utilized at the protected amino acid incorporation stage
    • Boc group cleaved prior to final formulation blending
    • Stringent removal of residual TFA and byproducts to achieve cosmetic purity

    Final product types

    • Anti-wrinkle and skin-firming peptide actives
    • Brightening peptide complexes
    • Cosmetic-grade peptide bulk for inclusion in finished skincare products

    5. Veterinary Peptide API Production

    Animal health pharmaceutical companies incorporate Boc-L-lysine as an essential intermediate for veterinary peptide API production. Its protected format ensures precise synthesis of sequences administered in injectable, oral, or topical animal formulations. Manufacturing QCs focus on minimizing cross-contamination and maintaining residue limits in accordance with animal drug safety standards.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practices for Veterinary Products
    • US FDA Guidance for Industry: CGMPs for Medicated Feed and Veterinary APIs
    • European Pharmacopoeia monographs on veterinary peptide APIs
    • Certificate of Suitability (CEP) applications for export

    Typical usage ratio

    • 0.95–1.05 equivalents per lysine residue, adjusted by animal species and dosage formulation
    • Ratio refined based on peptide chain contaminants profile

    Downstream process integration

    • Integrated in initial protected amino acid mixture for solid-phase synthesis
    • Boc removed during sequential deprotection prior to final chain release
    • Final APIs undergo sterile filtration and formulation for veterinary use

    Final product types

    • Veterinary injectable peptide APIs
    • Oral peptide-based animal treatments
    • Active peptide ingredients for topical animal health products
    Free Quote

    Competitive Boc-L-lysine 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.

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    Certification & Compliance
    More Introduction

    Boc-L-Lysine: Building Stability and Efficiency Into Peptide Synthesis

    Practical Precision in Chemical Manufacturing

    Many years go into optimizing a single synthetic step. Out on the production floor, every person working at our site understands how the right protecting group can shape the direction of a reaction, influence product yield, reduce purification headaches, and help clients keep their costs manageable. Boc-L-lysine sits at the intersection of practical process chemistry and modern biological applications, building value for those who need reliability, reproducibility, and clarity in their work.

    Our journey with Boc-L-lysine (Boc = tert-butoxycarbonyl) started from requests by researchers and production chemists who ran into unpredictable results with less consistent material. We learned early that minor variations in protecting group stability, moisture content, and purity impact peptide coupling outcomes and scale-up projects. Our batch-to-batch uniformity takes shape through careful raw material selection, in-process monitoring, and regular feedback from clients. Chemical plants, not distributors or trading houses, have to eat the cost of failed reactions. That sense of accountability pushes us to put real attention on every intermediate we ship.

    Essential Qualities for Research and Industry

    L-lysine, being a basic amino acid, comes with a side chain amine that reacts readily in peptide chemistry. Protecting this amine reduces side reactions and simplifies purification. Out of different protection strategies, the Boc group continues delivering robust performance in Fmoc/t-Boc based solid-phase and solution-phase peptide synthesis. Chemists know that solid-phase approaches—used for everything from laboratory peptides to preclinical therapeutic candidates—benefit from the stability and mild deprotection profile of Boc-L-lysine.

    When we talk with peptide developers, most highlight the need for materials that resist moisture pickup and decomposition during storage. Our Boc-L-lysine features a controlled particle size distribution, proven to reduce dusting and clumping during weighing and transfer. Careful drying and air-tight packaging further minimize hydrolysis. Product purity, confirmed by HPLC and NMR, consistently reaches above 99%. Impurities in the lot can wreak havoc downstream by generating unknown byproducts during synthesis and purification, so we take a zero-compromise approach.

    Meeting the Challenge of Peptide Synthesis

    Peptide coupling relies on the orthogonal protection of lysine’s α- and ε-amino groups. Boc-L-lysine brings selectivity that’s difficult to match by direct acylation—without its use, side chain acylation can reduce yield and add costly purification steps. Some might wonder why not just use Fmoc-lysine derivatives for everything. Yet applications employing mixed Boc and Fmoc strategies, especially those facing solubility or aggregation issues, find Boc-L-lysine invaluable.

    Solid-phase synthesis at manufacturing scale amplifies every detail. Minor inconsistencies in amino acid derivatives, water content, or residual solvents can translate to batch failures costing hundreds of thousands of dollars. Our commitment to process control evolved alongside feedback from teams scaling preclinical oligonucleotide and peptide APIs. Boc-L-lysine allows seamless integration with standard peptide-resin workflows, and our technical support helps optimize coupling and deprotection cycles using real-world plant data.

    How Boc-L-Lysine Stands Apart

    Many suppliers offer protected lysine derivatives, but very few actually control the upstream chemistry. Technical product managers often reach out after encountering inconsistent reactivity or unexplained impurities in their shipments—issues that trace back to third-party processors or poor storage conditions. Factory direct sourcing ensures traceability and transparency. End users sometimes underestimate the difficulties arising from repacked or relabeled material—volatile impurities evaporating off over time, or amorphous caking that ruins dosing accuracy.

    The Boc group on the lysine molecule blocks the ε-amine, leaving the α-amine free to couple, and we guarantee that selectivity with every batch. For custom protocols, some clients request specific salt forms or particle sizes for easier automation or specialized resins. We accommodate these requirements by managing all upstream and downstream production, packaging, and logistics. Since we see the material through every stage, we provide full support on troubleshooting—something third-party brokers rarely do.

    Insights From Daily Manufacturing Realities

    Reliable peptide synthesis starts at the warehouse. Every facility receives shipments of Boc-L-lysine that need to maintain stability over the storage period. Hygroscopicity, clumping, and batch segregation seem like simple warehouse issues but quickly snowball into thousands of dollars lost during make-up, batch splits, or reworking. Strict drying protocols, including low-temperature vacuum drying, keep product within target moisture ranges. Our packaging engineers worked with floor operators to develop resealable, moisture-barrier bags that stand up to repeated handling in both R&D and process suites.

    Another overlooked consideration comes from machine interface. Automated capsule dosing or feeder applicants benefit from free-flowing powders or fine granules. If product bridges or aggregates, it causes inconsistent feeding rates or force process shutdowns. Our quality improvement programs focus on both the technical—like rapid moisture testing and impurity screening—and the practical, like ergonomic packaging that reduces trace loss. Handling challenges described by operators feedback directly to our process chemists, who then adjust parameters to improve subsequent lots.

    Protecting-Group Chemistry: Balancing Strength and Lability

    Boc-L-lysine takes on a role far beyond that of a simple intermediate. In complex peptide assembly, stability under mildly acidic conditions paired with reliable removal under stronger acid creates flexibility in stepwise synthesis. Unlike CBZ or Alloc protection, Boc deprotection typically uses trifluoroacetic acid under controlled conditions—our technical support has advised both pharma and academic teams on fine-tuning these cycles for both safety and economy.

    Manufacturing brings realities like scale-up hazards, solvent recovery, and the ever-present risk from trace contaminations. Cross-contamination from incompletely protected lysine intermediates can show up as ghost peaks or unexplained elution shifts during peptide analysis. These issues rarely get traced back to the actual source material by non-specialists. Our background in analytical method development and process validation informs how we screen for even minor byproducts, so nobody faces surprises during regulatory audits.

    Customer Dialogues That Shape Product Development

    End users bring the sharpest feedback. Researchers scaling up peptides complain about one-to-one batch substitutions failing to match previous results, or unexpected issues like inconsistent coupling times or incomplete deprotection. Early on, one partner flagged difficulties dissolving our product in certain coupling reagents. Their feedback inspired a process overhaul—switching to finer particle size control, verified by laser diffraction, which improved solubility and dosing speed.

    Open conversations with both small molecule and peptide manufacturers press us to improve purity standards without pushing cost past market expectations. Balancing cost with quality means investing in robust in-line monitoring, not just end-of-line testing. Our continuous improvements came from actual plant data, not readouts from global distributors. By serving both pilot and kilogram-scale demands directly, we learn how day-to-day chemistry and logistics decisions ripple across whole projects.

    Comparisons to Related Products

    Some request Fmoc-L-lysine as an alternative, citing the milder deprotection conditions and compatibility with automated synthesizers common at larger academic and diagnostic labs. Fmoc derivatives excel where base-labile protection is preferable, but Boc-L-lysine suits protocols needing strong acid deprotection—often selected to work around sensitive side chains or minimize racemization risks. For solid-phase synthesis involving side-chain protecting groups like Mtt or Dde, Boc’s unique profile avoids overlap, reducing unwanted cross-reactions and cleanup steps.

    CBZ–protected lysine, another frequent comparison, deprotects under catalytic hydrogenation. This creates challenges for scale where hydrogen gas or precious metals present GMP or process hazard issues. Alloc and Dde protecting groups, while orthogonal, can introduce hard-to-remove byproducts from palladium or hydrazine reagents. Boc protection stands out as robust and economical, minimizing risk when throughput, cost, or regulatory risk is critical.

    Traceability and Transparency

    Full traceability sits at the core of every shipment. As a manufacturer, not a trading firm, our facility logs every raw material acquisition, production run, and analytical result. Customers can review archived batch records on request, or request technical support around product history, impurity profiles, or stability data. Many comments from quality control teams highlight the peace of mind that comes from working with a direct producer—eliminating the uncertainty of repackers, resellers, or opaque supply chains.

    Transparency helps de-risk projects. When investigators ask about origins of residual solvents or potential genotoxins, we can provide full upstream data, validated by regular in-house and third-party audits. Environmental and regulatory requirements keep tightening across countries, so we keep documentation and compliance systems agile. We never rely on inherited specifications; every analytical method is validated or adjusted against current industry standards and customer requirements.

    Supporting Reliable Workflows in Synthesis and Scale-Up

    Peptide and oligonucleotide producers often adjust synthetic protocols based on reproducibility, purification, and material-handling performance. Boc-L-lysine holds a place in projects ranging from neoantigen vaccine studies to engineered protein analogues, and even small-molecule peptide hybrids. Every batch we dispatch refines its own legacy—client feedback goes directly to our QA and process teams, ensuring critical QC checkpoints align with actual workflow demands.

    Failures in protected amino acid supply chains can cause month-long delays, missed clinical deadlines, or regulatory headaches. Long-term partners tell us that rapid, stable access to Boc-L-lysine supports everything from new R&D projects to validated GMP processes. Our willingness to adjust lot sizes, packaging forms, and purity levels matches the dynamic nature of pharmaceutical, biotech, or diagnostics companies—making us a resource rather than just a vendor.

    Solutions to Synthesis and Purity Challenges

    The cost of low-purity or unstable material appears not just in wasted raw material, but in downtime, rework, and missed windows for intermediate reactions. We address these needs by layering quality control into every step—from remote sensor-monitored humidity tracking to HPLC analysis of every batch against international reference standards.

    Process improvements often mean tightening moisture controls, swapping to more inert packaging, or streamlining shipping so product doesn’t linger in suboptimal conditions. We also support custom lot documentation and retain samples to enable root-cause investigations. When researchers spot a performance issue downstream, our technical and analytical team can reference the originating batch for deeper troubleshooting—closing the loop between manufacturing and application.

    Responsiveness and Ongoing Improvement

    Continuous improvement comes from real operator experience and customer reports, not just lab metrics. We seek out operator stories—how powders handled in glove boxes pack inappropriately, what happens when a container runs low, or which batches dissolve quickest. Feedback showing that newer packaging survives long-term storage spurred us to widen moisture-barrier adoption. Analytical teams worked directly with process operators on troubleshooting difficult batches, implementing tweaks that later become standard practice.

    Direct communication means clients explain their problem, and we work on the fix—whether it’s slightly finer granulation for a new dosing machine, a novel packaging format, or improved labeling to streamline compliance documentation. We maintain an open channel for all users of Boc-L-lysine, whether they’re running lab-scale syntheses or full GMP product runs, understanding that robust product support reduces all stakeholders’ risk.

    Final Thoughts: Boc-L-Lysine’s Place in Modern Chemistry

    The landscape of synthetic biology and peptide therapeutics keeps advancing. We stay grounded in the everyday needs of those who blend, dose, automate, validate, and troubleshoot reactions with Boc-L-lysine. Our experience comes not from trading catalog numbers, but from moving kilograms through real reactors, supporting chemists and engineers in their projects, and integrating customer feedback into continuous improvement cycles.

    Boc-L-lysine never remains static—its production, handling, and application evolve with client needs and changing regulatory environments. We treat every lot as an opportunity to build trust, reduce end-user headaches, and fuel progress in peptide chemistry. By bridging factory floor experience with the needs of innovators worldwide, we help ensure every synthesis step counts, every time.