|
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 | 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. |
Applications of N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-Arginine in Industrial ManufacturingAs 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&DContract 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
Typical usage ratio
Downstream process integration
Final product types
2. Peptide Reagent Manufacturing for Proteomics ConsumablesProducers 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
Typical usage ratio
Downstream process integration
Final product types
3. Custom Peptide API Intermediates for Biotechnology ProductionBiotechnology 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
Typical usage ratio
Downstream process integration
Final product types
4. Peptide-Based Fine Chemicals in Diagnostic ApplicationsCompanies 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
Typical usage ratio
Downstream process integration
Final product types
5. Reference Peptide Manufacturing for Pharmacopoeial StandardsCertified 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
Typical usage ratio
Downstream process integration
Final product types
6. Specialty Oligopeptide Production for Cosmetic Ingredient SectorProducers 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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive N-Fmoc-N'-(4-Methoxy-2,3,6-Trimethylbenzenesulfonyl)-D-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
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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."
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.
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.
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.
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.
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.