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Fmoc-D-Tyr(tBu)-OH

    • Product Name Fmoc-D-Tyr(tBu)-OH
    • Alias FMOC-D-TYR(OTBU)-OH
    • Einecs 259-415-2
    • 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

    943363

    Product Name Fmoc-D-Tyr(tBu)-OH
    Full Name N-α-9-Fluorenylmethyloxycarbonyl-D-tyrosine tert-butyl ester
    Molecular Formula C28H29NO5
    Cas Number 135716-65-5
    Appearance White to off-white powder
    Optical Purity D-isomer
    Protecting Groups Fmoc (N-terminal), tBu (side chain phenol)
    Solubility Soluble in DMF, DMSO, methanol
    Application Peptide synthesis
    Melting Point 152-158 °C
    Storage Temperature 2-8 °C
    Smiles CC(C)(C)Oc1ccc(cc1)[C@@H](NC(=O)OCC2c3ccccc3-c4c2cccc4)C(=O)O

    As an accredited Fmoc-D-Tyr(tBu)-OH factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle, tightly sealed with screw cap, labeled "Fmoc-D-Tyr(tBu)-OH, 5g." Features hazard symbols and lot number.
    Shipping Fmoc-D-Tyr(tBu)-OH is shipped in a tightly sealed container, protected from light and moisture, and typically kept at ambient or cool temperatures. Standard chemical shipping regulations apply, with appropriate labeling and documentation provided. It is packed to prevent damage during transit, ensuring product integrity and safety.
    Storage **Fmoc-D-Tyr(tBu)-OH** should be stored in a cool, dry place, away from light and moisture. Keep in a tightly sealed container under an inert atmosphere (e.g., nitrogen or argon) to prevent decomposition. Store at 2–8°C (refrigerator) for optimal stability. Handle in accordance with good laboratory practices, avoiding prolonged exposure to air and humidity.
    Application of Fmoc-D-Tyr(tBu)-OH

    Applications of Fmoc-D-Tyr(tBu)-OH in Industrial Manufacturing

    Fmoc-D-Tyr(tBu)-OH is a key protected amino acid derivative used by peptide synthesis companies, pharmaceutical active ingredient manufacturers, and biotech research suppliers. Downstream fields rely on its purity and robust protecting groups to maintain stringent standards during complex molecule assembly. The following sections provide application-specific detail for different industrial settings.

    1. Solid Phase Peptide Synthesis (SPPS) for Peptide Drug Development

    Pharmaceutical firms engaged in peptide active pharmaceutical ingredient (API) production require high-purity Fmoc-D-Tyr(tBu)-OH during automated SPPS. The material serves as a building block for introducing D-tyrosine moieties at specific sites in synthetic peptides, enabling improved bioavailability, metabolic stability, and receptor selectivity. Its side-chain tBu protection supports orthogonality in multi-step synthesis, reducing risk of deprotection overlap. Critical process controls focus on coupling efficiency and minimization of racemization at every cycle, typically under stringent GMP environments. Finished peptides undergo rigorous in-process and release testing for identity, purity, and residual solvents.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP <823> Peptides
    • Ph. Eur. monographs for peptide APIs
    • 21 CFR Part 210/211 (FDA cGMP)

    Typical usage ratio

    • 0.95–1.10 molar equivalents per peptide cycle
    • Adjusted based on resin loading and sequence complexity
    • Standard 1:1 amino acid to growing peptide chain
    • Slight excess for difficult coupling positions as needed

    Downstream process integration

    • Added in initial amino acid charge step on solid support
    • Activated using carbodiimide or uronium salt chemistry
    • Participates in iterative coupling and deprotection cycles
    • tBu group removed during final global deprotection before purification

    Final product types

    • Synthetic peptide APIs (e.g., hormones, enzyme inhibitors, receptor agonists)
    • Generic peptide drug substances
    • Investigational new drug (IND) candidate peptides
    • Peptide reference standards

    2. Manufacturing of Peptide-Based Diagnostics

    Diagnostic reagent producers utilize Fmoc-D-Tyr(tBu)-OH for controlled site incorporation of D-tyrosine in synthetic peptides, particularly where resistance to enzymatic degradation is required (e.g., laboratory immunoassays, diagnostic ELISA controls, and biosensor calibration peptides). Precise synthesis is essential to ensure batch-to-batch consistency and functional stability when immobilizing these peptides onto assay surfaces. The raw material's tBu-protected side chain resists undesired modification during process steps involving surface modification or fluorophore labeling.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices—Quality Management
    • CLSIs GP44-A4 for production of in vitro diagnostic (IVD) reagents
    • EU Regulation 2017/746 on In Vitro Diagnostic Medical Devices (IVDR)
    • US FDA 21 CFR 820 QSR (for IVDs)

    Typical usage ratio

    • 1.0 molar equivalent per D-Tyr-containing sequence position
    • Customized loading based on the number of D-amino acid sites
    • 0.98–1.05 ratio preferred for automated platforms
    • Validation runs may use higher excess at site-specific substitutions

    Downstream process integration

    • Charged onto solid support during peptide chain assembly
    • tBu group retained for selective functional group protection during label coupling
    • Deprotected after all modifications complete
    • Purified peptides conjugated to assay surfaces post-synthesis

    Final product types

    • Diagnostic assay peptides (e.g., ELISA/CLIA controls, calibrators)
    • Biosensor peptide ligands
    • Coated microwell and microarray peptides
    • Labeled reference standards

    3. Research-Grade Peptide and Protein Engineering

    Biotechnology laboratories engaged in custom peptide and protein analog synthesis depend on Fmoc-D-Tyr(tBu)-OH to build modified peptide libraries, enzyme substrates, and model proteins with enhanced or altered properties. In these advanced research applications, the material enables the incorporation of D-Tyr residues to probe stereochemical effects on protein folding, receptor interaction, and enzymatic resistance. The flexibility of tBu-protected side chains allows for late-stage functional group modification before final global deprotection. Strict analytical protocols are used to confirm absence of sequence errors and ensure site-specific incorporation of protected D-Tyr.

    Industry compliance standards

    • ISO 9001:2015 quality management for research reagents
    • GLP (Good Laboratory Practice) for traceable synthesis
    • OECD Guidelines for Testing of Chemicals
    • Standard operating procedures (SOPs) for analytical testing

    Typical usage ratio

    • 1.0–1.2 molar equivalents per desired library position
    • Higher ratios (1.2–1.5) for complex or branched peptide synthesis
    • Scaled based on intended length of peptide chain
    • Optimized for automated robotic peptide synthesizers

    Downstream process integration

    • Charged in situ on automated peptide synthesizers or manual SPPS setups
    • Integrated with combinatorial library generation methods
    • tBu group often cleaved in the final deprotection/mass spec confirmation step
    • Downstream derivatization for functional studies after purification

    Final product types

    • Custom research-grade peptides
    • High-throughput peptide libraries
    • D-Tyr-modified enzyme substrates
    • Protein analogs for structural biology

    4. Synthesis of Modified Peptide Excipients for Drug Delivery

    Pharmaceutical excipient manufacturers employ Fmoc-D-Tyr(tBu)-OH in the synthesis of specialty peptide excipients that modulate solubility, stability, or controlled release behavior in parenteral and oral drug formulations. The D-tyrosine residue, introduced using SPPS flows, can reduce proteolytic cleavage and prolong peptide lifetime in formulation matrices. Precise handling and integration of the tBu-protected derivative safeguards critical hydroxyl functions during co-ligand attachment and microencapsulation chemistries. Process engineers monitor for complete removal of Fmoc and tBu groups prior to excipient blending with APIs, in accordance with pharmacopeial impurity and residual solvent thresholds.

    Industry compliance standards

    • USP <1078> Good Manufacturing Practices for Bulk Pharmaceutical Excipients
    • Ph. Eur. 5.1.1 for excipient microbial quality
    • FDA Inactive Ingredient Database (IID) guidelines
    • ICH Q3A/B on impurities/residual solvents

    Typical usage ratio

    • 0.98–1.05 molar equivalent per D-Tyr modification site in excipient
    • Calculated as a proportion of total amino acid content in excipient peptide
    • Usage may scale in applications requiring multiple D-Tyr residues
    • Adjusted based on desired rate of excipient-provided stabilization

    Downstream process integration

    • Added at site-specific steps during excipient peptide chain assembly
    • Side-chain protected tBu group maintained during microparticle formation or PEGylation
    • Final deprotection and purification prior to excipient-API blending
    • In-process QC to confirm chemical identity and absence of protecting groups in released excipient

    Final product types

    • Peptide-based stabilizers for injectable biopharmaceuticals
    • Microencapsulation agents for oral drugs
    • Controlled release peptide excipients
    • Sterile bulk peptide excipient powders
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    Certification & Compliance
    More Introduction

    Fmoc-D-Tyr(tBu)-OH: Precision Protected Amino Acid for Advanced Peptide Synthesis

    Time-Tested Practices in Manufacturing

    Working hands-on with peptides, we understand the value of reliable building blocks. Fmoc-D-Tyr(tBu)-OH stands out in our production, thanks to years spent fine-tuning each step from raw material to finished product. Using the Fmoc protecting group for the α-amino function and tert-butyl for the phenolic hydroxyl, this derivative supports strict control in peptide assembly. Each batch reflects deliberate process control—from the selection of chiral starting materials to the monitoring of reagent purity at each stage of synthesis. By relying on ourselves for each reaction, we achieve the stereochemical integrity required by demanding peptide projects.

    Specification and Experience in Manufacturing

    Producing Fmoc-D-Tyr(tBu)-OH isn’t just about following a recipe. It’s about troubleshooting subtle variances—sometimes as simple as a shift in reaction temperature, sometimes as involved as protecting a sensitive batch from atmospheric moisture during recrystallization. Our team monitors the product’s melting point, optical rotation, and chemical purity with tools proven by decades in the lab. NMR and HPLC tell the story behind every lot number. We look for a white to off-white crystalline powder, real purity measured by more than just the numbers in the certificate of analysis. If any discoloration or off-note appears, we go back to the drawing board and start with the raw materials.

    Usage Realities in Peptide Manufacturing

    Fmoc-D-Tyr(tBu)-OH finds its importance in solid phase peptide synthesis. The Fmoc group survives standard peptide coupling reactions and removes under mild basic conditions, without disturbing other critical functionality in the growing peptide chain. The tert-butyl group on the tyrosine side chain gives extra protection, blocking unwanted side reactions during chain assembly and deprotection cycles. In our practice, this minimizes risk of side-chain oxidation or bifurcation, sparing hours that would have been spent isolating difficult-to-remove byproducts. Peptide scientists recognize how one poorly protected amino acid will compromise yield and purity for an entire batch—something we have witnessed ourselves. Choosing this product helps, as every gram delivers peace of mind for both early-stage R&D and industrial manufacturing runs.

    Why D-Amino Acids Matter in Modern Platforms

    The D-configuration on tyrosine flips the stereochemistry relative to natural proteins. Incorporating D-forms is a standard approach to resist protease digestion and alter peptide conformation. From our experience serving pharmaceutical labs, Fmoc-D-Tyr(tBu)-OH appears in custom peptides for enzyme resistance or mirrored protein studies. Our years supplying universities and startups taught us: every stereochemical switch in a molecule changes both structure and downstream performance. Customers expect we know the handling differences between D- and L-isomers—our practices reflect this, from chiral column screening in quality control to strict batch segregation on our production floor. Careless substitution or cross-contamination means downstream batches end up unusable—a risk we never allow.

    Key Differences that Speak to Value

    Comparing Fmoc-D-Tyr(tBu)-OH to similar protected tyrosines highlights the kind of trade-offs chemists face daily. Fmoc-L-Tyr(tBu)-OH would be used for natural sequence peptides, but the D-form clearly targets specific modification or resistance needs. If the tert-butyl group is omitted, side reactions compete during the assembly cycle and purification steps become more difficult. Some chemists still opt for Boc protection strategies, based on their solid phase protocol or to avoid certain deprotection conditions, but the Fmoc group streamlines parallel synthesis and automation—a valuable time-saver for anyone using advanced synthesizers. Our familiarity with these protection strategies means we advise partners on the best fit for each job, drawing from the mistakes and successes we have seen firsthand over years of process support.

    Obstacles in Production and Solutions from the Manufacturer’s Perspective

    It’s easy to overlook small details, but these become pain points at scale. We deal with the tedium of repeated recrystallizations and grinding to the correct particle size. The tert-butyl group brings in another layer of complexity by increasing hydrophobicity, complicating dissolving and weighing. We combat this by drying the product under vacuum and grinding it in controlled conditions. Every new partnership brings fresh feedback on what matters most to the user—sometimes it’s solubility, other times it’s flow characteristics in automated dispensers. These aren’t just theoretical; we have responded to peptide plant engineers after one sticky batch slowed production. Our improvements stem from constant feedback with chemists who use our products in daily research, not distant distributors guessing at laboratory needs.

    Scientific Rigor Beyond Certificate of Analysis

    Regulatory expectations grow every year, but even before such rules, our internal quality system demanded high purity and batch traceability. Each lot of Fmoc-D-Tyr(tBu)-OH is tracked from its raw amino acid precursor through all modification steps, building a record of compliance for audits as well as customer confidence. We learned early that firms working on pharmaceuticals expect electronic documentation, clean-room packaging, and full validation of both process and raw material supply. Our investment in these areas reflects the demands of our most innovative customers, many of whom cannot sacrifice quality for price or convenience.

    Supply Chain Insights from a Maker’s View

    Raw material shortages, price swings, and logistical delays have all challenged us at some point. We maintain redundant suppliers for key precursors like D-tyrosine and reagents for Fmoc and tert-butyl protection. Multi-country sourcing has protected our production schedule through everything from holiday slowdowns to shipping bottlenecks. Once, a blizzard in Europe delayed a major L-amino acid source; our D-amino acid reserves kept customer orders on track. We do not gamble with short-term savings at the cost of future supply gaps. By running our own inventory, we give our clients stability to plan advanced peptide pipelines —every gram we supply arrives with a history we can explain, not just a manufacturer’s label.

    Continuous Improvement through Direct User Feedback

    Open channels to synthetic chemists and process engineers provide a direct line to understand market needs. Over the years, input from universities, pharma labs, and diagnostics companies inspired practical improvements: tamper-evident bottles, extra batch certification, and detailed physical property data sheets for automated systems. Our technical support goes beyond FAQ guides—real people answer with insight grounded in experience, drawn from a manufacturing floor rather than a customer service script. We keep adjusting product specs and batch controls as new demands emerge from evolving research areas. These dialogues helped us align our offerings with the real-world challenges users face, keeping waste down and reproducibility high.

    Trends in Peptide Chemistry Affecting Fmoc-D-Tyr(tBu)-OH

    Peptide-based drugs and diagnostics now permeate clinical and research spaces everywhere. Chemists increasingly design in D-residues to address stability, selectivity, and metabolic challenges. New technologies for automated multichannel synthesis have raised the bar: every amino acid derivative must meet both batch- and dose-to-dose consistency. Through collaborations with biotech developers, we see how deviations as small as 0.1% impurity change the outcome of high-throughput screens or biologic candidate selection. That’s why we invest heavily in both people and instrument calibration to match these stringent modern standards. Fmoc-D-Tyr(tBu)-OH finds itself adopted in everything from personalized therapeutics to research into artificial enzymes—each project putting its own spin on established chemistry but never lowering expectations for reliability.

    Environmental and Safety Considerations

    Manufacturing specialty amino acids brings its own set of safety and environmental challenges. Protecting reactive intermediates from moisture means maintaining proper ventilation and spill control. We’ve built exhaust systems and solvent capture methods that exceed basic local guidelines, learning through costly mistakes how easily a vented batch or improper storage will lead to waste and exposure risks. All liquid waste streams from tert-butylation and Fmoc protection steps pass through in-house treatment before disposal. Our approach reflects lessons learned along the way—the direct result of handling synthesis reagents and hazardous materials ourselves, not farming out the process. This lets us serve clients needing cGMP-grade material, but it also maintains the kind of stewardship we want for our own employees and environment.

    Compatibility with Custom Synthesis and Specialized Protocols

    Some projects demand non-standard coupling agents, nonpolar solvents, or unique combinations of deprotection and cleavage conditions. We work directly with formulation scientists, sending demo samples, gathering application notes, and following up until the product fits both their process and regulatory standards. Fmoc-D-Tyr(tBu)-OH sits in peptide libraries requiring wide parameter ranges—feedback from those projects means our deliveries contain advice on reported solvent compatibility, as well as any batch-specific recommendations when anomalies arise. Maintaining open lines of communication, we adapt protocols together instead of forcing rigid documentation on a flexible science.

    Case Studies: Lessons from the Factory Floor

    Years ago, we adjusted a purification step that reduced crystallization time, saving our team hours per batch with no loss in quality. Stepping into the lab ourselves, we troubleshoot issues scientists report: pellets sticking to the vessel after freeze-drying, static clumping slowing down automated dispensers, or uneven bulk density throwing off gravimetric feeds. Chemists send us feedback on solubility in DMF versus DCM, on how the product handles in robots and multi-channel pipettors. Each insight lands directly in our process documentation and informs process changes if necessary. This ongoing cycle of input and improvement defines how we keep advancing the quality and applicability of Fmoc-D-Tyr(tBu)-OH without resting on old recipes.

    Collaborative Approach with Research and Production Teams

    Manufacturers play a different role from traders: we have to anticipate the direction of research, scale protocols, and adapt to new usage scenarios quickly. Our storerooms contain both kilo-scale and R&D-scale inventory because projects shift rapidly from feasibility study to preclinical production. Sometimes customers want the entire batch history traced; sometimes only small multi-gram samples fit their pilot runs. Our team tracks and labels everything to match the speed of peptide innovation, but grounded in the discipline that comes from handling hazardous reagents and high-value research products in real time.

    Challenges Facing the Field and Long-Term Solutions

    Peptide chemistry never stops evolving, but what hasn’t changed is the demand for certainty. Supply chain shocks, emerging contaminants, and shifting regulatory frameworks force adaptation daily. We invest in cross-training our staff so anyone can troubleshoot both chemical and logistical problems—a necessity for manufacturers keeping pace with rapid change. As new methodologies like flow chemistry and ultra-fast automated synthesis come online, adjustment periods expose weak points in even the best process. We continuously engage with process chemists and regulatory auditors to re-map procedures, always seeking ways to strengthen reproducibility and cut unnecessary steps. The resulting resilience means that Fmoc-D-Tyr(tBu)-OH serves industries with requirements worlds apart—from start-up research efforts to commercial pharmaceutical synthesis.

    Final Impressions: Making the Difference Count

    As makers, our investment is twofold: the raw chemistry behind Fmoc-D-Tyr(tBu)-OH and the experience learned day-to-day serving those who depend on it. Confidence in each gram’s quality comes from seeing its path through the plant and discussing its use with each new scientist entering the field. We have staked our reputation on products like Fmoc-D-Tyr(tBu)-OH, believing that direct experience, honest communication, and technical accountability give our customers more than a commodity—they get a trusted resource for their evolving peptide missions. The drive to refine, support, and stand behind this specialty amino acid isn’t a passing policy for us; it’s a direct response to the real and recurring challenges of modern peptide chemistry, experienced firsthand on our factory floor.