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N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine

    • Product Name N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine
    • Alias Fmoc-D-Arg(Pmc)-OH
    • Einecs 807-104-5
    • 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

    548562

    Product Name N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine
    Chemical Formula C32H38N4O7S
    Molecular Weight 622.73 g/mol
    Purity Typically ≥ 98%
    Appearance White to off-white solid
    Storage Temperature 2-8°C (refrigerated)
    Cas Number 123332-54-1
    Solubility Soluble in DMF, DMSO, and slightly in methanol
    Protecting Groups Fmoc (N-terminal), 4-Methoxy-2,3,6-trimethylbenzenesulfonyl (N'-guanidino)
    Chirality D-configuration
    Application Used in peptide synthesis
    Synonyms Fmoc-MeSO2-D-Arg-OH
    Stability Stable under recommended storage conditions

    As an accredited N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied as a white solid in a 1 gram amber glass bottle, sealed with a screw cap, labeled with product and safety information.
    Shipping The chemical N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Standard shipping is via ground or air, in compliance with relevant hazardous materials regulations. Proper labeling and documentation are included to ensure safe and compliant transportation.
    Storage Store N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine in a tightly sealed container under dry, inert atmosphere, such as nitrogen or argon. Keep at 2–8°C, protected from light and moisture. Avoid exposure to heat, sources of ignition, and incompatible substances such as strong acids and bases. Handle with appropriate protective equipment in a well-ventilated area.
    Application of N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine

    Applications of N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine in Industrial Manufacturing

    As a recognized producer, we supply N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine to a focused range of synthesis and process industries. Below we detail the main industrial downstream sectors using this compound, illustrating actual requirements, necessary compliance standards, formulation ratios, validated process integration, and precise end-product forms.

    1. Protected Peptide Synthesis in Pharmaceutical R&D

    Contract research and pharmaceutical formulation labs employ this protected D-arginine derivative during solid-phase peptide synthesis to achieve site-specific modifications and enhance peptide sequence selectivity. Fmoc-based temporary protection ensures accurate stepwise elongation while sulfonyl groups improve the yield and purity of arginine-containing peptides under mild deprotection conditions. Manufacturers employ defined protocols to ensure that product quality meets investigational drug submission requirements for new peptide-based compounds.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • USP General Chapter <1047> for peptide substances (where applicable)
    • EMA guidelines on synthetic peptide APIs
    • ISO 9001:2015 quality management for chemical processing

    Typical usage ratio

    • 12–22 mol% of protected amino acid component depending on target peptide sequence; ratio adjusted for resin loading and stepwise coupling scale

    Downstream process integration

    • Utilized at the N-terminal elongation stage in automated SPPS reactors
    • Enters coupling cycle with specific activation reagents
    • Removed selectively during Fmoc deprotection steps for purity optimization
    • Sampled for in-process QC by HPLC and mass spectrometry

    Final product types

    • Research-grade and GMP-grade pharmaceutical peptides
    • API intermediates for antihypertensive and antithrombotic drug candidates
    • Investigational small-length peptide analogues
    • Reference standards for clinical trial submissions

    2. Peptide Reagent Manufacturing for Proteomics Consumables

    Producers of specialized proteomics kits incorporate this D-arginine-based amino acid during sequence-controlled synthesis to enable targeted modification or labeling in mass spectrometry workflow standards. Its sterically protected form ensures minimal side-chain reactions while allowing for precise peptide building blocks, crucial for generating calibration reagents and isotopic standards used in high-throughput proteomics.

    Industry compliance standards

    • ISO 13485:2016 for production of diagnostic system reagents
    • REACH Regulation (EC) No 1907/2006 for laboratory reagents
    • CFR Title 21 Part 820 (Quality System Regulation, US for kit components)
    • SDS documentation and shipping rules per GHS/OSHA standard

    Typical usage ratio

    • 8–18 mol% of resin loading; exact dosage depends on targeted peptide length and labeling frequency needed

    Downstream process integration

    • Added at key protection steps during custom synthesis in proprietary kit development lines
    • Integrated before isotopic or fluorescent labeling reactions to control modification positions
    • Batch testing with LC-MS confirmation for final sequence identity
    • Packaged after freeze-drying under nitrogen to maintain reagent integrity

    Final product types

    • Protease cleavage standards for mass spectrometers
    • Quantitative peptide calibrators
    • Isotopically labeled peptide mixes
    • Labeled peptide fragments for kit inclusion

    3. Custom Peptide API Intermediates for Biotechnology Production

    Biotechnology firms preparing complex non-racemic peptide APIs integrate this building block for selective D-arginine protection in multi-step synthetic protocols. The electron-rich sulfonyl protection stabilizes side chains during hydrogenolysis and enzymatic cleavage, enhancing the processability and batch homogeneity of advanced API intermediates essential for biotherapeutic development.

    Industry compliance standards

    • GMP according to ICH Q7 and EudraLex Volume 4, Part II, for biochemical intermediates
    • FDA guidance for synthetic steps in peptide-based drug substance manufacture
    • ICH Q6A for specifications and impurity profiling
    • ISO 14644-1 controlled environment for high-purity processes

    Typical usage ratio

    • 15–25 mol% in protected amino acid pools; ratio varies with target API batch size and purity goals

    Downstream process integration

    • Functions at the pre-assembly phase during amino acid pool preparation
    • Feeds into semi-automated SPPS and hybrid liquid-phase batch synthesis
    • Remains protected during initial cleavage; selectively deprotected for targeted enzymatic modifications
    • QC monitoring by UPLC and NMR for conformance to batch release

    Final product types

    • D-arginine-containing peptide API intermediates
    • Modified peptide segments for biotherapeutic assembly
    • Intermediates for advanced wound healing research
    • Biosimilar peptide fragments for process validation

    4. Peptide-Based Fine Chemicals in Diagnostic Applications

    Companies producing peptide fine chemicals for diagnostic substrates utilize this material as a highly specific protected amino acid to construct synthetic substrates for enzyme assays and biomarker detection reagents. The steric protection ensures defined N-terminal configuration, supporting high sensitivity and reproducibility in downstream assay performance critical for clinical diagnostics.

    Industry compliance standards

    • ISO 13485 (Medical Devices & Diagnostics)
    • European Pharmacopoeia 10.0 monographs on peptide reference substances
    • FDA's Quality System Regulation (QSR)
    • RoHS (EU Directive 2011/65/EU) for diagnostic device chemicals

    Typical usage ratio

    • 9–14 mol% among protected amino acid input; set ratio determined by required degree of substitution for specific chemiluminescent or colorimetric substrate design

    Downstream process integration

    • Added at the protected amino acid assembly stage in automated synthesizers
    • Post-assembly chemical cleavage yields the active assay substrate
    • Included in lyophilized assay kits after QC validation and batch release testing
    • Assessed for stability in long-term storage studies

    Final product types

    • Synthetic enzymatic substrates for ELISA and chemiluminescent assays
    • Colorimetric peptide reagents
    • Clinical biomarker detection substrates
    • Peptide standards for instrument calibration

    5. Reference Peptide Manufacturing for Pharmacopoeial Standards

    Certified chemical reference material producers employ this protected D-arginine in the controlled synthesis of pharmacopoeia-standard peptides. It provides unambiguous definition of protected sites and enables reproducible batch manufacturing crucial for issuing qualified reference substances distributed to analytical laboratories and regulatory agencies worldwide for method calibration and validation.

    Industry compliance standards

    • ISO/IEC 17025:2017 accredited laboratory requirements
    • European Pharmacopoeia/USP/JP reference standard guidelines
    • SOP-driven batch record and traceability documentation
    • GDP (Good Distribution Practice) for certified reference materials

    Typical usage ratio

    • 10–20 mol% within custom sequence synthesis, closely controlled for each reference batch

    Downstream process integration

    • Integrated at the single amino acid coupling step with documented protection group retention
    • QC evaluation by peptide map analysis and absolute mass spectrometry
    • Vialed and labeled for reference use upon achieving homogeneous peptide standard status
    • Long-term stability studies simulate regulatory laboratory conditions

    Final product types

    • Pharmacopoeial reference peptides for QC labs
    • ISO-compliant peptide calibration standards
    • Lot-traceable analytical reference substances
    • Certified secondary standards for regulatory analysis

    6. Specialty Oligopeptide Production for Cosmetic Ingredient Sector

    Producers of cosmetic grade oligopeptides utilize this protected D-arginine compound to build sequence-identical peptides for high-end topical formulations, including skin conditioning peptides with modified arginine sites for enhanced bioactivity. The protective groups permit stepwise, selective peptide assembly while protecting sensitive backbone and side chains from undesired modifications during high-throughput batch processing.

    Industry compliance standards

    • ISO 22716:2007 GMP for cosmetic manufacturing
    • Cosmetic Ingredient Review (CIR) safety assessment guidelines
    • EU Regulation (EC) 1223/2009 on cosmetic products
    • IFRA standards for ingredient quality when applicable

    Typical usage ratio

    • 8–12 mol% in protected amino acid mix, with exact ratio fine-tuned by cosmetic peptide length and desired functional group exposure

    Downstream process integration

    • Feeds into solid-phase or solution-phase cosmetic peptide synthesis
    • Selectively deprotected prior to final hydrolysis and purification
    • Tested for residual solvent and contaminant levels in compliance with cosmetic ingredient dossiers
    • Bulk packed for direct use in peptide concentrate or serum manufacturing

    Final product types

    • Synthetic bioactive cosmetic peptides
    • Topical skincare ingredient blends containing D-arginine residues
    • Peptide active concentrate solutions
    • Aesthetic treatment oligopeptide complexes
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    Certification & Compliance
    More Introduction

    N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine: Focused Reliability in Peptide Synthesis

    Craftsmanship in Chemical Manufacturing

    Working in the chemical industry, we approach every compound with a hands-on understanding that comes from years spent in the lab and the plant. N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine stands as an example of how precision and careful process control create a reagent that consistently meets the tight demands of peptide synthesis. Making the right protecting group and configuration available for researchers and pharmaceutical teams means we can enable reliable results in downstream processes.

    What Sets This Compound Apart

    Building blocks for peptide synthesis rarely offer a simple journey. N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine goes farther than standard protected amino acids because our process retains stereoisomeric purity and provides stable reactivity without introducing side-reactions. There’s no room for half-measures in the approach, since even subtle impurities or inconsistent Fmoc-protection can derail an entire synthetic sequence. Handling sensitive groups like the sulfonamide requires high skill, starting with raw material quality and running through purification steps dialed in by skilled operators who know how to spot the difference between practical and theoretical chemistry.

    Model and Specifications—A Practical View

    At our manufacturing site, every batch starts with real-time monitoring. Specs for our product aren’t arbitrary; they reflect the accumulated insight from hundreds of runs and subtle process tweaks. We deliver N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine as a well-defined crystalline solid, offering a purity level that meets the needs of demanding organic chemists—typically above 98% by HPLC. Each lot is analyzed for trace water content, residual solvents, and optical purity. Chiral HPLC confirms the D-stereoisomer. We understand the downstream cost of variability; every specification ties back to a step in our workflow, not just to theoretical limits in textbooks.

    Working in a manufacturer’s shoes, every deviation or impurity brings real headaches. If an end customer ends up with a subpar coupling yield or sees unexpected side products, it reflects not only on the specific lot, but on the reliability of the synthetic design as a whole. Purity, steric configuration, and functional group stability aren’t abstract numbers for us—they define whether pioneering research succeeds or stalls.

    Unique Functional Features

    The value in this molecule springs from its protecting groups. The Fmoc group shields the amino function during peptide synthesis, enabling the widely used Fmoc-strategy in solid-phase peptide assembly. The 4-methoxy-2,3,6-trimethylbenzenesulfonyl group on the guanidino side chain manages the chemical reactivity, preventing premature side-reactions. Some users ask, “Can I swap out the sulfonyl protection or use standard Fmoc-Arginine?” We answer: not if you want a precise, robust route with clean results. The chosen side-chain protection resists cleavage under most conditions, so your deprotection and coupling steps proceed without hiccups.

    Years of feedback from pharma and academic customers guide our batch protocols. The robustness of this double-protected D-Arginine derivative allows it to fit seamlessly into automated peptide synthesizers just as well as hand-assembled solid-phase protocols. For peptide designs where the D-configuration provides enhanced stability against proteolytic degradation, or for use in modern peptidomimetic drug projects, it’s one of the most straightforward ways to ensure your arginine residue behaves just the way you intend up to the final deprotection.

    Understanding Application in Peptide Science

    Real experience in chemical synthesis shapes how we see the compound in action. In our own process development, inconsistent derivatives forced long troubleshooting sessions, rerunning syntheses, and adding unnecessary purification steps. By offering N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine with high purity and clear batch records, our customers avoid these traps. For peptide designers, incorporating the D-amino acid residue alters both structure and biological activity. Therapeutics built with D-Arginine show improved stability profiles, a key asset during preclinical studies or formulation work.

    We’ve noticed an uptick in demand from groups focused on antimicrobial peptides, peptide vaccines, and enzyme-resistant peptide drugs. Incorporating D-Arginine with this protection scheme adds a layer of control that enables novel structure-activity studies. For medicinal chemists, being able to count on the same behavior, lot to lot, lets them focus on what matters—biological results, not manufacturing flaws.

    Differences From Other Protected Arginine Forms

    Plenty of amino acid derivatives circulate in the market, but the differences often become painfully clear only under the demands of production-level synthesis. The sulfonyl-protected D-Arginine distinctly outperforms simpler forms, especially those using easily-cleaved protecting groups. In our production runs, we found certain alternatives led to partial side-chain deprotection during mild base treatments or left trace protecting residues after final cleavage. That shows up not only as yield losses, but as additional purification challenges, especially if the final peptide targets therapeutic grade or high-throughput screening.

    Some who started with standard Fmoc-D-Arg(Pbf)-OH reported peptide products contaminated by stubborn sulfonyl residues, which skew analytical results in purity or mass spec. The mesitylenesulfonyl group (4-methoxy-2,3,6-trimethylbenzenesulfonyl) holds up better to common deprotection protocols, resulting in sharper HPLC profiles and fewer cleanup artifacts. In our real-world output, switching to this derivative helped researchers save entire weeks on post-synthetic purification.

    Consistency Shaped by Manufacturing Experience

    Only time on the production line teaches the true importance of batch repeatability. The process conditions we use—temperature controls, reagent chases, and purification with repeated crystal washes—grow from years of actual troubleshooting. Equipment maintenance, supply chain controls, and training all fold into preventing batch-to-batch drift. When we spot small variances, the technical team reviews every production parameter, sometimes halting a run and reworking a batch to meet what we know our end users expect.

    Our customer technical support teams keep open lines to process chemists at pharma plants and university labs. Feedback cycles highlight not just what worked, but where further improvements hit practical roadblocks. By refining reaction times or solvents, we continuously push toward ever-sharper purity and performance, supported by analytic trends over hundreds of sample runs. Down the line, our warehouse and logistics staff deal with the practical side: safe, dry, contamination-proof packaging and consistent, predictable delivery times.

    Challenges in Scale-Up and How We Handle Them

    Scaling up specialty amino acid derivatives brings its own pain points. Minor inefficiencies or contamination that go unnoticed in gram-scale R&D become significant hurdles at the kilo scale. Our in-house chemists recognized early on that Fmoc removal, protecting group stability, and by-product management all behave differently at plant scale. For example, large reaction vessels require calibrated mixing and temperature ramping to prevent cold spots, which can lead to partial reactions and off-color products.

    Our team adopted in-process controls that catch these issues during the run—not after. By direct sampling at staging points, we catch incomplete reactions before they become end-lot variability. This hands-on vigilance isn’t theoretical; it saves reprocessing costs and keeps users from facing unpredictable impurities. As a direct manufacturer, our pride comes from hearing users comment that "this batch runs just like the last one," or "we didn’t need extra purification steps this time around."

    Safety, Integrity, and Environmental Commitment

    Manufacturing specialty protected amino acids involves responsible chemical management. Handling the mesitylenesulfonyl group means personal protective equipment for operators and carefully contained reaction environments. Waste streams receive the same attention as the final product. Investing in solvent recovery and secure containment for side-products lowers environmental burden and helps us meet both local and international guidelines.

    We train operators not just on routine procedure, but on why each safety step matters in practice. Real safety comes from hands-on vigilance, not from reminders in a manual. Digging into incident records led us to implement finer dust-control measures and sealed container transport inside the plant. By focusing on safety at every step, from raw material intake to final kilo-batch shipping, we protect both staff and the reputation hard-won by years of consistent supply.

    Lessons Learned—Practical Solutions to Common Problems

    Years of production runs teach lessons that can’t be found in published protocols. Overdrying during final product isolation produced static cling, which led to losses and handling headaches; a tweak to the drying cycle fixed that. Switching solvent systems for crystallization altered particle size, impacting filtration speed. Subtle changes in starting material grade sometimes threw off reaction rates or led to color issues. The solution always comes down to hands-on observation, real-time data, and honest assessment of what worked and what needs adjustment.

    We encourage end users to share feedback alongside their purchase orders—sometimes small details about dissolution or coupling behavior help us further refine what we offer. Over the past decade, collaboration between our manufacturing chemists and research users helped us minimize dust formation, maximize physical stability in storage, and keep our products performing reliably even in hot or humid warehouse conditions.

    Supporting Scientific Progress

    With deeper investment in research, peptide-based therapeutics keep gaining ground—in antibiotic resistance, metabolic disorders, and cancer signaling interruption. The need for robust, versatile, and pure protected amino acid derivatives never fades. We’ve watched the conversation move from simple Fmoc-protected amino acids to highly functionalized forms that keep up with evolving research. High-purity D-Arginine derivatives like this one become irreplaceable for building complex, selective, and stable peptide backbones.

    Our role doesn’t stop at the manufacturing gate. We take pride in being a resource for technical troubleshooting and process design. Whether helping design a strategy for prolonged coupling, maximizing load efficiency on a resin, or tracking down unlikely by-products, our crew shares practical advice rooted in experience. As synthetic targets get more challenging, our own operations get smarter, leaner, and more responsive to outlier results.

    Anticipating Future Needs

    Research goals keep advancing. In response, our manufacturing lines constantly evolve to support faster, greener, and more flexible production. Investment in cleaner solvent systems, smarter in-line analytics, and new purification technologies positions us to respond as regulatory expectations for peptide APIs tighten. As more users opt for D-amino acid-containing peptides, especially for therapeutic and diagnostic uses, the importance of stereochemical integrity and reliable protection only increases.

    Looking ahead, we focus on transparency and continuous improvement. The industry’s trend toward digital batch tracking and regulatory digitalization blends naturally with our own ethics of detailed documentation and traceability. Every successful project, every consistent delivery, adds to the base of trust between us and the research community.

    A Final Word from the Manufacturing Line

    Compounds like N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine bring out the best in technical production—complexity, precision, and measurable benefit for the users. True peace of mind in a chemical purchase doesn’t come from a catalog description or a spec sheet. It grows out of a transparent manufacturing process, clear technical feedback, and honest partnership between supplier and scientist. Each batch that leaves our doors represents not just another product, but the combined experience, learning, and pride of a crew dedicated to supporting breakthroughs in peptide science.