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HS Code |
665112 |
| Product Name | Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester |
| Cas Number | 120717-99-7 |
| Molecular Formula | C23H25NO6 |
| Molecular Weight | 411.45 |
| Purity | ≥98% |
| Physical State | Solid |
| Appearance | White to off-white powder |
| Solubility | Soluble in DMF, DMSO, and dichloromethane |
| Storage Temperature | 2-8°C |
| Protecting Groups | Fmoc (N-terminal), tBu (side-chain beta-carboxyl) |
| Optical Activity | D-isomer |
| Application | Peptide synthesis |
| Melting Point | 111-115°C |
| Synonyms | Fmoc-D-Asp(OtBu)-OH |
As an accredited Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed HDPE bottle labeled "Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester, 5g," featuring hazard symbols, batch number, and storage instructions. |
| Shipping | Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester is shipped in tightly sealed containers under ambient or cool, dry conditions to prevent moisture and light exposure. Packaging ensures safety and chemical stability during transit. Handle and store according to material safety data sheet (MSDS) recommendations. Expedited and temperature-controlled shipping is available upon request. |
| Storage | Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester should be stored in a tightly sealed container at 2-8°C (refrigerator temperature), in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Avoid exposure to light and heat. Ensure proper labeling and keep away from sources of ignition. Handle under an inert atmosphere if possible. |
Applications of Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester in Industrial ManufacturingAs a dedicated manufacturer of specialty amino acid derivatives, we produce Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester for integration into advanced peptide synthesis workflows and pharmaceuticals. Below, explore its industrial deployment across key downstream manufacturing scenarios, with each section reflecting authentic use cases and technical requirements encountered by end producers in regulated sectors. 1. Custom Peptide Synthesis for Pharmaceutical APIsDrug substance manufacturers incorporate this protected D-Asp derivative for solid-phase peptide synthesis (SPPS) of active pharmaceutical ingredients, primarily when synthesizing complex peptide drugs that require site-specific incorporation of D-amino acid residues. It reliably introduces the protected D-aspartic acid moiety, supporting efficient elongation of the peptide backbone without side-chain racemization or unwanted deprotection, which maintains the fidelity needed for regulatory-compliant peptide therapeutics. Industry compliance standards
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2. Synthesis of Peptide-Based Diagnostic AgentsProducers of molecular diagnostic kits and in vitro diagnostic (IVD) reagents utilize this material in the controlled assembly of peptide-based markers and substrates, particularly where resistance to enzymatic degradation is required. The beta-tert-butyl protection facilitates selective deprotection strategies during marker or probe synthesis, improving batch-to-batch reproducibility and quality compliance demanded by clinical laboratories. Industry compliance standards
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3. Manufacture of Modified Peptide Research ToolsBiotechnology and contract research organizations turn to this compound for the production of D-amino acid-containing peptides used in structural biology, enzyme interaction studies, and receptor mapping. Here, precise side-chain protection and compatibility with automated synthesizers ensure accurate study of chirality and side-chain-dependent phenomena critical for protein engineering and interaction mapping. Industry compliance standards
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4. Assembly of Peptidomimetic IntermediatesSpecialty chemical manufacturers employ this building block in advanced organic synthesis routes directed at peptidomimetic intermediates. The compound’s stable tertiary butyl ester and Fmoc protection withstand multistep organic transformation and allow controlled release of the carboxyl group at late-stage synthesis, which is crucial for scaffolds intended for therapeutic or agrochemical research. Industry compliance standards
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5. Design of D-Amino Acid Peptides for Cosmetic IngredientsCosmetic active ingredient producers integrate the protected D-amino acid derivative when designing non-standard peptides for anti-aging and skin-conditioning agents, particularly those engineered for resistance to skin peptidases. Its role in the SPPS process allows introduction of non-natural chirality to strengthen peptide stability, which helps formulators meet targeted dermal bioactivity profiles demanded by dermo-cosmetic brands. Industry compliance standards
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Manufacturing Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester, also known as Fmoc-D-Asp(OtBu)-OH, belongs to a set of specialty amino acids that play a key role in solid phase peptide synthesis. Few outside our field realize how much care, experience, and vigilance go into producing a molecule like this. Chemical identity can often be summarized with a catalog number—here, F33480—but as manufacturers, we always think in terms of material purity, process reproducibility, and consistency at bench and scale.
We select D-enantiomers only after confirming absolute stereochemical purity. Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester comes from our long practice of resolving racemic mixtures and managing chiral pool starting materials. Every lot comes from a single route: we protect the alpha-amine with Fmoc, install a tert-butyl ester at the beta-carboxyl, and keep the side chain from racemizing through careful temperature and pH control.
We do not see these steps as routine. Any deviation in the Fmoc-protection or tert-butyl esterification means an off-target byproduct, and mistakes in chiral control end up costing weeks of rework. Every stage gets sampled and analyzed by HPLC and NMR at multiple checkpoints. Over time, our adjustments—solvent exchange, catalyst tweaks, cleanup procedures—have cut byproduct formation significantly and made purification more robust for scale-up, which supports custom prep needs and multikilogram orders.
It's easy to lose sight of the physical aspects in a clean electronic catalog, yet each bottle comes out of months of hands-on work and full traceability from raw input to packed powder. Customers request detailed batch records because they expect operations to run smoothly when switching suppliers. For us, each specification—color, solubility, water content, melting point—is checked repeatedly and reported directly from our lab.
Most users see HPLC purity and enantiomeric excess listed in data sheets. Our Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester regularly tests above 98% chemical purity with enantiomeric purity upwards of 99%. Every batch comes as a white or near-white powder, which signals absence of oxidation or breakdown, and we monitor for residual solvents below detection limits of gas chromatography. Customers in the peptide research field or pharmaceutical intermediate synthesis expect no less.
Yield and crystallinity feel like abstract metrics but are grounded in process control. Reproducibility means not just making a clean product, but also making sure scale-up does not bring side reactions that emerge only in large reactors. Our procedures start in 100-gram trials before moving to full-scale batches, and successful scale-up always translates to less loss at purification, better downstream cost, and improved availability for time-sensitive orders.
Amino acid derivatives like Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester have a purpose: building peptides where every amino acid sits in a fixed configuration. Ongoing research into D-amino acid-containing peptides grows rapidly. Peptide chemists prefer the Fmoc group for N-protection because it comes off gently with piperidine, leaving the beta-carboxyl tert-butyl ester intact through the assembly. This property enables selective deprotection and is compatible with standard coupling protocols, which limits epimerization, a critical factor for biological function in chiral molecules.
The D-isomer version turns up in pharmaceutical research, especially for resistance to enzymatic degradation—an essential feature in peptide-based therapeutics. Many drugs and research tools depend on the precise orientation of these building blocks. Fmoc-D-Asp(OtBu)-OH offers stability both in storage and during solution-phase workups, reducing waste and extra steps.
Customers often ask about racemization risk. In practice, the combination of Fmoc- and OtBu-protection suits most coupling protocols and limits base-catalyzed chiral scrambling. We share real-world coupling examples and highlight any abnormal interaction with carbodiimide, HBTU, or HATU methods. Backed by our internal data, we recommend specific solvents and additives for maximum retention of stereochemistry and coupling efficiency.
Synthetic chemists can choose from several forms: Fmoc-D-Asp(OtBu)-OH, Fmoc-D-Asp(OBzl)-OH, Boc-D-Asp(OtBu)-OH, and unprotected aspartic acid are all valid tools but each comes with trade-offs. We have seen in our facility how the beta-tert-butyl ester holds up better in acidic environments than OBzl (benzyl) esters, which require catalytic hydrogenation for removal. OtBu groups come off smoothly with TFA (trifluoroacetic acid), and the removal creates less risk for over-reaction or byproducts.
Boc-protected versions serve some applications, yet the Boc group deprotects under milder acid and does not always match the Fmoc workflow preferred worldwide in modern peptide chemistry. We optimize starting material quality and protective group stability for every derivative produced. Our experience shows that customers working with solid-phase protocols, especially those using Fmoc/tBu chemistry on polystyrene and PEG resins, rely on Fmoc-D-Asp(OtBu)-OH for its selectivity and convenience.
Peptide length and residue composition challenge different protection strategies. Our technical support teams get direct feedback from production-scale users and research teams, and that affects our process refinement and QC focus. Every comparison made with competitive samples comes down to yield, purity, and control over byproducts—because every synthetic peptide's bioactivity or research result depends on confident building block performance.
Every batch tells a story about feedback loops and learning. For years, reagents like Fmoc chloride and tert-butyl alcohol used to vary by source, so our material input controls are strict. We pre-screen vendors for impurities, and incoming QC includes not just standard melting point and IR analysis, but also LC-MS to catch less obvious contaminants. Employees know the cost of shortcuts, because peptide founders don’t just want “good enough”—they demand reproducible results, every time.
Moisture and storage conditions come up every winter and summer. Tert-butyl esters readily hydrolyze in the presence of strong acids and water, so finished Fmoc-D-Asp(OtBu)-OH gets dried and packed under nitrogen. Even slight moisture raises the risk of sticky clumps, poor flow, and eventual degradation, and our team keeps glassware and storage lines clean and dry at every batch stage.
Researchers need quick delivery, but every urgent request can collide with real-world process risks. We prioritize scale-out to keep buffer inventories on hand and limit the chance of rushed final drying or packaging. We hear from our customers: supply chain consistency matters most, especially for peptide-makers running long projects or scaling for regulatory filings. For every pound on the shelf, we've held back a few hundred grams for re-test—a practice that helped customers weather pandemic-era choke points and global freight chaos.
Waste minimization also shapes our day-to-day planning. Our plant engineers monitor wash water, organic residues, and recovery for every protection step. Over the last decade, process improvements have cut our solvent and reagent consumption by more than a third, trimming costs and keeping hazardous output in check. This reduces exposure for both staff and customers, aligns with ongoing environmental reporting requirements, and answers customer questions about sustainability and compliance.
Solid-phase and solution-phase peptide chemistries each present their own wrinkles. As a manufacturer, we learn from both sides: working with discovery researchers who might need only a few grams, and supporting API process chemists who plan out 100-gram or kilogram campaigns for IND or NDA submissions. Customizations often include alternate packing sizes, specialized documentation for audit trails, or technical documents for regulatory review, all supported by our batch traceability.
We field questions every week about compatibility with coupling reagents and resin types. For our Fmoc-D-Asp(OtBu)-OH, we help troubleshoot real-world coupling challenges—sticking resin, incomplete deprotection, or unexpected chromatograms—from groups trying to push synthesis to longer and more complex peptides. We also work with existing customers to adapt purity standards to their particular validation needs, sometimes testing for specific low-level byproducts or providing fresh stability data from internal or third-party labs.
Knowing the chemistry in depth changes how feedback is handled. Analytical data can hint at problems with stirring, temperature, or mixing rates. We welcome feedback, because any customer headache with handling, dissolution, or side reaction becomes a focal point for future process change. Open lines with process teams, instrument vendors, and even logistics partners mean that our Fmoc-D-Asp(OtBu)-OH has been through trials and improvements far beyond its original formulation.
Global peptide chemistry trends—a surge in therapeutic peptides, new delivery technologies, and regulatory tightening—continuously increase the demands for specialty amino acid derivatives. Manufacturing Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester for these evolving needs means anticipating not only purity and quality, but also more transparent supply chains, full regulatory documentation, and robust customer support. Our decades of accumulated experience make a difference every batch, whether for milligram pilot runs or tens of kilograms headed for clinical trial peptide syntheses.
Batch-to-batch consistency and reliable record-keeping—the so-called “paper trail”—are prized by research and pharma customers expecting compliance with ISO or GMP-like standards, even if formal GMP certification does not apply. Regular audits, process walk-throughs, and sample retention demonstrate that our Fmoc-D-Asp(OtBu)-OH is not just a commodity. Each challenge addressed, from improved purification steps to contingency planning for raw material shortages, improves customer outcomes.
Companies new to peptide development often underestimate the value of a direct manufacturer relationship until a delay or technical setback exposes the downside of commodity or trader-only supply. Every year, more customers shift to direct sourcing, seeking not only documentation and certificates but the assurance that comes from working with a manufacturer willing to share technical know-how, troubleshooting support, and process transparency. We see this industry trend growing: buyers no longer settle for the least expensive option—they want reliability, accountability, and direct access to problem solving.
True to the core, every sample of Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester we send represents weeks of hands-on testing, internal review, and customer feedback. Our chemists, analysts, and technical sales teams share decades of experience with protecting group chemistry, peptide synthesis, and supply chain logistics. Every bottle carries results from collaborative chemistry: cleaner peptides, less waste, and smoother scale-up for every user, whether in early research or late-phase clinical work.
In the crowded world of chemical suppliers, direct manufacturers bring substance behind the promise. Every step in delivering Fmoc-D-Aspartic Acid Beta-Tert-Butyl Ester comes from decades learning how to make, test, and deliver high-performance amino acid derivatives. With each order and each round of feedback, the process refines, so customers can trust these building blocks not just on spec sheets, but in the real-world business of innovative science.
We look forward to continuing the partnership, sharing technical knowledge, and helping researchers and developers unlock the full range of what custom-protected amino acids can do. Fmoc-D-Asp(OtBu)-OH stands as more than just a product in our catalog—it’s a tested and proven solution purpose-built for today’s peptide science.