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

Fmoc-L-Arginine

    • Product Name Fmoc-L-Arginine
    • Alias Fmoc-Arg-OH
    • Einecs 259-393-4
    • 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

    777556

    Product Name Fmoc-L-Arginine
    Chemical Formula C20H23N5O4
    Cas Number 72020-25-4
    Appearance White to off-white powder
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Solubility Soluble in DMF, DMSO
    Usage Peptide synthesis
    Protecting Group Fmoc (9-Fluorenylmethyloxycarbonyl)
    Optical Rotation [α]D20 +27° (c=1, DMF)
    Synonyms Fmoc-Arg-OH
    Stability Stable under recommended storage conditions

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

    Packing & Storage
    Packing The packaging for Fmoc-L-Arginine, 5 grams, is a tightly sealed amber glass bottle with a printed chemical label for identification.
    Shipping Fmoc-L-Arginine is shipped in secure, tightly sealed containers to protect against moisture and contamination. The packaging complies with chemical safety regulations and includes appropriate labeling and documentation. Shipments are typically made via regulated carriers with temperature and handling controls, ensuring the product’s stability and integrity during transit.
    Storage Fmoc-L-Arginine should be stored in a cool, dry place away from direct sunlight and moisture. Keep the container tightly closed when not in use. Store at 2-8°C (refrigerator temperature) for optimal stability. Protect from light and incompatible substances such as strong acids, bases, and oxidizing agents. Use with appropriate personal protective equipment in a well-ventilated area.
    Application of Fmoc-L-Arginine

    Applications of Fmoc-L-Arginine in Industrial Manufacturing

    Fmoc-L-Arginine serves as a high-purity protected amino acid essential to numerous advanced industrial processes. Acting as a specialty reagent in synthetic chemistry, it helps downstream manufacturers meet regulatory, quality, and process efficiency requirements for innovating in pharmaceuticals, peptides, diagnostics, and functional biomaterials.

    1. Solid Phase Peptide Synthesis (SPPS) in Pharmaceutical Manufacturing

    Peptide drug producers rely on Fmoc-L-Arginine as a critical building block during solid phase peptide synthesis, particularly for the construction of arginine-rich therapeutic peptides and oligopeptides. The Fmoc protection group prevents undesired side reactions on the guanidino group during chain elongation. Optimizing the coupling ratio and deprotection steps ensures high yields and purity for active pharmaceutical ingredients (APIs) under GMP protocols. Stringent batch traceability and analytical control maintain pharmaceutical compliance throughout the peptide's lifecycle, including for generic and innovative medications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <1095> Pharmaceutical Peptides
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EU EudraLex Volume 4 Guidelines

    Typical usage ratio

    • Equimolar to other protected amino acids, typically 1:1 per residue position
    • Can adjust charge ratio (1.05–1.10 equivalents) for difficult couplings or high arginine content peptides

    Downstream process integration

    • Loaded onto peptide synthesizer resin via automated or semi-automated SPPS protocol
    • Fmoc group removed post-coupling using 20% piperidine in DMF
    • Final API undergoes purification via preparative HPLC
    • Residual solvents and protecting groups removed during post-synthesis treatment

    Final product types

    • Synthetic peptide APIs (e.g., glucagon-like peptide analogs, gonadotropin-releasing hormone agonists)
    • Peptide hormone drugs
    • Peptide-based diagnostic reagents
    • Generic pharmaceutical peptides

    2. Custom Peptide and Diagnostic Probe Synthesis

    Contract research organizations, diagnostics firms, and academic labs integrate Fmoc-L-Arginine for the synthesis of custom peptides, labeling probes, and antibody production controls. Its application centers on high-throughput parallel synthesis, with the purity and fidelity of the protected arginine residue directly affecting assay sensitivity and reproducibility. The material’s compatibility with automated instrument platforms enables batch consistency required for regulatory validation of diagnostic test kits and research reagents. Quality documentation, including COA and QC batch records, ensures compliance for diagnostic submissions.

    Industry compliance standards

    • ISO 13485:2016 for Medical Devices and In Vitro Diagnostic (IVD) Manufacturing
    • CLSI EP05 Assessment Protocols
    • EU In Vitro Diagnostic Regulation (IVDR)
    • OECD Good Laboratory Practice (GLP)

    Typical usage ratio

    • 1.0 equivalent per arginine residue in peptide sequence
    • Adjusts up to 1.2 equivalents for sequences prone to aggregation or low substitution resin loads

    Downstream process integration

    • Charged into multichannel automated or manual peptide synthesizer vessels
    • Coupling stages followed by parallel Fmoc removal cycles
    • Desalt and purify using flash chromatography or HPLC
    • Final lyophilization and aliquoting for QC and validated testing

    Final product types

    • Synthetic peptide diagnostic calibrators
    • Epitope mapping peptides for monoclonal antibody development
    • Fluorophore-labeled peptide probes
    • Reference standards for LC-MS based analysis

    3. Biomedical Functional Materials and Hydrogels

    Advanced biomaterial manufacturers incorporate Fmoc-L-Arginine into peptide-based hydrogel systems for tissue engineering scaffolds, drug delivery platforms, and wound healing matrices. The arginine residue’s side chain offers ionic and hydrogen bonding functionality, while the temporary Fmoc group enables selective assembly of multi-component biomaterials. Manufacturers follow ISO, USP, and medical device GMP guidelines from raw material preparation and peptide assembly to final device packaging and sterilization. Material selection and traceability are documented for audit and biocompatibility review.

    Industry compliance standards

    • ISO 10993-1 Biocompatibility Evaluation of Medical Devices
    • USP <1031> Biologic Materials Guidelines
    • 21 CFR Part 820 (Medical Device Quality System Regulation)
    • ISO 14644-1 Cleanroom Standards

    Typical usage ratio

    • 5–25 mol% of total peptide content, depending on gel strength and charge properties
    • Adjust according to hydrogel formulation requirements for porosity and crosslinking

    Downstream process integration

    • Dosed into hydrogel precursor peptides during solid-phase or liquid-phase synthesis
    • Fmoc deprotection managed post-assembly to enable gelation via self-assembly or crosslinking chemistry
    • Hydrogel processed under sterile, controlled conditions and shaped for final application
    • Biocompatibility and release testing as per device class

    Final product types

    • Bioresorbable wound dressings
    • Tissue regeneration matrices
    • Injectable drug delivery hydrogels
    • Cell encapsulation scaffolds

    4. Research-Grade Peptidomimetics and Proteomics Reagents

    Biotechnology companies and proteomics labs employ Fmoc-L-Arginine for synthesizing peptidomimetics, enzyme substrates, and isotopically labeled peptides. Its utility in controlled stepwise synthesis enables the assembly of arginine-containing analogs for mass spectrometry standards, enzyme activity assays, and inhibitor screening. Processes demand attention to raw material integrity, trace metal content, and sequence fidelity to avoid assay interference, following documentation and traceability practices per research and analytical standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Laboratory Reagents
    • GLP (OECD Principles of Good Laboratory Practice)
    • REACH Regulation (EC) No. 1907/2006 for laboratory chemicals in the EU
    • CFR 21 Part 58 (FDA Good Laboratory Practice for Nonclinical Laboratories)

    Typical usage ratio

    • 1 equivalent per arginine residue for custom synthesis
    • Quantities range from milligram scale (analytical standards) to gram scale (screening libraries)

    Downstream process integration

    • Incorporated at the residue-selective coupling stage during Fmoc/t-Bu peptide synthesis protocols
    • Fmoc group removed by base-catalyzed deprotection before chain extension
    • Peptidomimetics cyclized or modified at N- or C-terminal as per assay design
    • QC performed via HR-MS and analytical HPLC before release

    Final product types

    • Synthetic peptide libraries for high-throughput screening
    • Mass spectrometry calibration standards
    • Enzyme activity assay substrates
    • Stable isotope-labeled internal standards
    Free Quote

    Competitive Fmoc-L-Arginine 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

    Introducing Fmoc-L-Arginine: Value in Every Batch

    The Role of Fmoc-L-Arginine in Peptide Synthesis

    Fmoc-L-Arginine holds an essential place among protected amino acid derivatives relied on for solid-phase peptide synthesis (SPPS). In the lab, reproducibility and purity decide project timelines and research credibility. Having spent years behind reactors and purification columns, we have watched countless projects hinge on this exact intermediate. Its guanidino group, a unique feature distinguishing arginine, demands thoughtful protection. The Fmoc group shields the α-amine, while Pbf—one of the most reliable protecting groups—guards the side chain. The result is a building block built to endure the demands of automated synthesis while giving chemists confidence in each coupling step.

    Model and Specifications Matter

    We manufacture Fmoc-L-Arginine with a specific focus on peptide laboratories that push for consistent, high-quality yields. Our most widely used model, Fmoc-L-Arg(Pbf)-OH, is a white to off-white crystalline powder. Typical purity for this product exceeds 98% by HPLC, with water content kept below 1.0%—standards deliberately maintained because trace impurities in peptide work often stall progress or force expensive purifications downstream. Pack sizes suit research or production: smaller bottles cater to scale-up, while large-format packaging serves kilogram requirements for contract manufacturing organizations.

    Years of running peptide syntheses informed several improvements in production and quality control. We rely on surveillance at every stage, from raw material acceptance to final QC release, ensuring batch-to-batch consistency. Each lot comes with an analytical report: identity confirmed by NMR and MS, purity and residual solvents checked by HPLC and GC, and affirmation of Pbf protection by IR and reaction monitoring. Chemically, the Fmoc-protected amino acid stands up to standard activation reagents including HBTU, HATU, and DIC/Oxyma. This builds reliability into SPPS cycles that involve multiple deprotection and coupling steps—no missed couplings or premature side chain deprotection across our experience with commercial clients.

    How Fmoc-L-Arginine Performs in the Real World

    In the world of peptide science, arginine frequently presents a challenge. Its side chain is basic and often causes aggregation or side reactions, especially during resin cleavage and purification. The Pbf-protected form we manufacture addresses these hurdles by offering high solubility in DMF and NMP and resistance to acidolytic cleavage conditions found at the final stage of peptide release. Through thousands of syntheses—from short peptides to complex, branched structures—our product’s performance translates into fewer truncated sequences and minimal guanidination of neighboring residues.

    The level of solubility and reactivity matter greatly. We have matched our salt and hydrate form selection for optimal dissolution in common solvents, minimizing time spent coaxing material into solution. This matters in high-throughput or automated syntheses, where every extra step costs labor or machine time. Chemists tell us that reliable Fmoc-L-Arg(Pbf)-OH lets them keep focus on scale-up or optimization, not troubleshooting resin swelling or precipitation.

    Comparisons: What Sets Fmoc-L-Arginine Apart

    Choosing Fmoc-L-Arginine from a manufacturer and not an unknown distributor gives research teams access to documentation and instant answers when scale-up issues emerge. This laboratory-to-laboratory line of communication exists because we also run peptide projects for our in-house R&D, not just external customers. Fmoc-L-Arginine from an established supplier eliminates problems like inconsistent moisture or variable purity, even across large-scale batches. We have seen firsthand how inconsistency in any one lot can ripple across complex peptide projects, costing time and budget.

    Some sources offer alternative protecting groups, but these frequently compromise cleavage efficiency or residue compatibility. For example, the nitro or tosyl analogs can limit final-stage removal yields, or introduce side products requiring additional chromatography. The Pbf group’s acid lability remains standard for most challenging peptides. Researchers have repeatedly confirmed that the Fmoc strategy—using Pbf-protected arginine—remains the preferred combination for purity and reliability, whether for manual synthesis or high-throughput automated setups.

    Addressing the Big Picture: Why Purity and Source Matter

    As a chemical manufacturer, we have seen the ecosystem of peptide production evolve rapidly. There was a time when researchers tolerated some variance in amino acid derivatives, especially for proof-of-concept work. That flexibility disappeared as expectations for reproducible drug candidates and peptides for clinical studies rose. Many regulatory submissions now require clear traceability back to original manufacture—not just paperwork from a distributor. We have built our process around transparency in every batch, with audits and documentation available for regulatory or academic verification.

    We recognize that some partners attempt to cut costs by sourcing from less expensive intermediaries. In almost every case, the loss comes not just as yield but also as troubleshooting cycles and revalidation costs. A single low-purity batch cascades into weeks of analytical investigation—chromatographic ghosts, unexpected cleavage fragments, or unexplained sequence deletions. The peace of mind our teams achieve by relying on our own Fmoc-L-Arg(Pbf)-OH means faster project advancement and fewer “unknowns” at QC checkpoints. In this industry, that counts for more than any paper savings at the procurement level.

    Usage Patterns in Industry and Research

    Fmoc-L-Arginine, in its Pbf-protected format, finds wide uptake in projects as diverse as fundamental cell biology, immune research, and peptide API production. In clinical peptide manufacturing, regulatory requirements for audit trails often extend to original certificate of analysis, batch manufacturing records, and process validation details. Because we have lived through agency inspections, we design every batch to stand up to such scrutiny. For research applications, speed remains the differentiator. Providing quick delivery, with every lot supported by full analytical data, means we see our products in global laboratories running vaccine candidates, molecular probes, and bioactive peptide analogs all within the same year.

    In-house peptide chemists face demanding schedules and shifting product targets, so the reliability we build into Fmoc-L-Arginine allows projects to pivot without additional risk. From pilot-scale lots measured in grams to routine campaigns counted in kilograms, the product profile remains unchanged: consistent Fmoc and Pbf protection, no batch-to-batch variation, and rapid, helpful technical support on questions relating to solubility, side reactions, or coupling optimization.

    Addressing Common Concerns: Stability and Storage

    Stability sits as a top concern every peptide chemist considers, especially given the value of pure building blocks. Moisture and oxygen rapidly degrade Fmoc-protected amino acids under improper conditions. Our teams store Fmoc-L-Arginine under dry nitrogen, in sealed, double-layered polyethylene bags. Every package includes a factory moisture indicator so lab personnel can confirm product integrity on arrival. Transport vehicles use temperature tracking to confirm journeys stayed below required thresholds, protecting both small research shipments and commercial bulk orders.

    Our stability studies, tracking purity at periodic intervals, inform every storage and packaging protocol. These measures arose from real-world project lessons: rushed unpacking or careless inventory handling would sometimes lead to slow color changes or weakened coupling efficacy. We work closely with partners and clients to share best practices, including proper aliquoting and desiccant use, and rapid transfer into dry boxes. The more closely protocols match our recommendations, the more reliably critical projects succeed.

    Trends in Peptide Development Highlighting Key Needs

    Active pharmaceutical peptides and diagnostic probes keep growing in complexity, bringing more attention to every building block. We have watched the trend move toward longer sequences, higher charge densities, and frequent inclusion of arginine residues for cell penetration or activity optimization. Fmoc-L-Arginine, by design, meets the demands these applications create. Our synthesis method began with solution-phase protocols, progressing over time to automated solid-phase platforms. At each step, we adjusted crystallization, purification, and drying conditions based on stability and coupling outcomes.

    In recent years, clients have asked for extra documentation—trace metals analyses, endotoxin assessments, and bioburden results. These parameters now appear regularly in our CoAs and in batch files for reference. We do not add these tests as afterthoughts; they exist because our peptide users showed, laboratory by laboratory, that these values affect biological readouts and long-term project value.

    Collaboration and Knowledge Sharing Strengthen Outcomes

    Producing Fmoc-L-Arginine is not a purely technical exercise. We engage with academia and industry to share improvements, troubleshooting discoveries, and early warnings about potential incompatibilities. Some collaborative projects have uncovered lot-specific influences on optical purity or minor decomposition pathways affecting long syntheses. By tracing batches and collecting feedback, we closed those gaps. The closeness of information sharing supports research at every scale, strengthening reproducibility from both supplier and research sides.

    We regularly host technical sessions on protected amino acid handling, resin selection, and process optimization for recurring customers and research collaborators. These community efforts make an impact: within months of introducing a new solubility-enhancing pre-mix, a dozen different peptide facilities improved their synthesis throughput. Such gains reinforce our commitment to keeping every Fmoc-L-Arginine batch reliable and accessible.

    Solving Industry Challenges: Reliability Over Hype

    People working in chemistry recognize marketing language fast. Claims about “superior performance,” “next-generation” derivatives, or “breakthrough yields” matter little once an impurity or side product slips through. Years of working in the field taught us to focus on the things that really matter for a manufacturer: tight control over intermediates, refusing shortcuts on purification, and immediate response if a customer reports an out-of-spec experience. Our factory direct support reduces lag in solving these rare challenges; you talk directly to scientists solving the same problems in their own lab work.

    Feedback from large-scale partners centers on this point. Bulk customers need uninterrupted processes, not just initial samples. Maintaining lots in reserve, with overlapping quality control reviews, allows research organizations to deliver consistent commercial lots under global agency standards. Documentation is prepared to satisfy both GMP and research grade expectations whenever required.

    Environmental and Safety Considerations

    Manufacturing and handling Fmoc-L-Arginine in large quantities shines a light on sustainability and safety. Our facility has shifted to solvent recovery systems, lowering overall solvent use and recycling DMF and DCM used in protected amino acid manufacturing. Wastewater accountability keeps us in step with local and national standards; these steps come not as external requirements, but as a reflection of our long-term outlook on chemical processing. Technicians rely on thorough safety protocols—dedicated air handling and PPE enforcement keep output free from cross-contamination, and work areas safe for extended operation.

    Improvements in drying, crystallization, and final packaging mean higher lot yields with less material waste. Our analytical group continues to develop VOC monitoring, so air and water leaving the plant match both regulatory limits and community expectations. Even if this level of investment pulls resources, it means research customers downstream never worry about residual traces of regulated solvents in the chemicals they receive.

    Looking Forward: Fmoc-L-Arginine as a Trusted Standard

    Fmoc-L-Arginine now serves in everything from proof-of-concept peptides to clinical stage APIs. Its role in research continues to expand, with methods evolving for longer sequences, higher loadings on resin, and new cleavable linkers. Being committed to transparency and collaboration puts us in front of changing needs—feedback from global partners guides every modification in synthesis and quality procedures.

    We keep improving every touchpoint: tighter batch documentation, real-time traceability, and direct technical exchange. Scientists invest too much time in each experiment to gamble on unknowns. Experience shows, year after year, that sequence success builds on reliable, high-purity Fmoc-L-Arginine. Every team and every facility counts on that, and so do we.