|
HS Code |
824627 |
| product_name | Boc-L-Asp-OH |
| chemical_name | tert-Butoxycarbonyl-L-aspartic acid |
| synonyms | N-Boc-L-aspartic acid |
| CAS_number | 13139-17-8 |
| molecular_formula | C9H15NO6 |
| molecular_weight | 233.22 |
| appearance | White to off-white powder |
| purity | Typically ≥98% |
| solubility | Slightly soluble in water, soluble in DMF and DMSO |
| specific_rotation | [α]20/D +18° to +22° (c=1, DMF) |
| melting_point | 119-123 °C |
| storage_temperature | 2-8°C |
| function | Amino acid derivative for peptide synthesis |
| protecting_group | Boc (tert-butoxycarbonyl) |
| chiral_purity | L-isomer |
As an accredited Boc-L-Asp-OH factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Boc-L-Asp-OH is supplied in a sealed, labeled amber glass bottle containing 25 grams, with hazard and storage information clearly indicated. |
| Shipping | Boc-L-Asp-OH is shipped in tightly sealed containers to protect it from moisture and contamination. It is typically transported at ambient temperature unless otherwise specified. The packaging complies with standard chemical safety regulations, ensuring secure transit. Shipping documentation includes safety data sheets, and handling precautions are clearly indicated to ensure safe delivery. |
| Storage | **Boc-L-Asp-OH** should be stored in a tightly sealed container, away from moisture and direct sunlight. It is best kept at 2–8 °C (refrigerator temperature) in a cool, dry place. Protect from heat and strong oxidizing agents. Proper labelling and handling procedures should be followed to ensure safety and maintain product integrity. |
Applications of Boc-L-Asp-OH in Industrial ManufacturingAs a trusted manufacturer, we supply Boc-L-Asp-OH for complex applications in life sciences and advanced materials. Used for its stability, purity, and protective properties, this intermediate enables consistent downstream synthesis across peptide therapeutics, specialty APIs, diagnostic reagents, and fine chemical custom manufacturing. Below, we present clearly defined application scenarios, detailing compliance frameworks, usage parameters, integration methods, and representative end products. 1. Peptide Therapeutics SynthesisBoc-L-Asp-OH serves as a backbone-protected aspartic acid building block in regulated peptide manufacturing, ensuring controlled deprotection and minimal racemization during solid-phase or solution-phase synthesis. Its use directly affects chain elongation fidelity and final product activity. Process chemists select it for proprietary formulations which demand high batch consistency and traceability—from initial loading on resins to large-scale purification and lyophilization for injectable peptide APIs. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Custom API Intermediate ManufacturingOur Boc-L-Asp-OH enables large-scale production of advanced pharmaceutical intermediates, particularly as a protected amino acid unit in the assembly of modified peptide-linker payloads, cytotoxic conjugates, and small molecule drugs with aspartyl residues. By controlling protection-deprotection flow with Boc group stability, process engineers ensure precise functionalization and minimize undesired isomerization—even in challenging multi-step, multi-solvent operation cycles. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Diagnostic Peptide Synthesis for In Vitro AssaysMolecular diagnostics manufacturers use Boc-L-Asp-OH as an essential protected amino acid in assembling peptide markers and substrates for diagnostic immunoassays, enzyme activity tests, and LC-MS-based quantification standards. High purity is necessary to prevent background noise in analytical outputs. Integration is closely monitored to guarantee lot-to-lot performance, especially for substrates requiring exact aspartic acid placement to ensure desired antigenicity or cleavage specificity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Fine Chemicals and Bioconjugate ManufacturingProducers of functionalized materials and bioconjugates introduce Boc-L-Asp-OH as a precision building block in projects requiring differentiated amide bond formation or site-specific functional group introduction. For example, it enables controlled derivatization of dendritic polymers, nanoparticles, or multi-arm PEGs, underpinning the synthesis of both analytical standards and novel bioactive formulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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As a manufacturer focused on amino acid derivatives, we recognize Boc-L-Asp-OH as a core intermediate for researchers and process chemists. Our roots run deep in peptide chemistry, so we witness daily how the right protective groups make a world of difference. Boc-L-Aspartic acid, or Boc-L-Asp-OH, carries a clear role in introducing aspartic acid with reliable N-alpha protection, letting users choreograph their syntheses with confidence.
Each batch of our Boc-L-Asp-OH comes stabilized with a precisely applied tert-butyloxycarbonyl (Boc) group at the alpha-amino position. Many in the industry reach for this format since it strikes a practical balance between stability and deprotection ease—crucial for stepwise and solution-phase assembly. From our perspective, having made this compound for years, the quality demands start with raw materials; we use only pharmaceutical-grade L-Asp, freshly sourced and handled with care right up until Boc installation.
Chemists using solid-phase synthesis often remark that the hallmark of trustworthy Boc-L-Asp-OH shows up in reproducible coupling and clean deprotection. Experience tells us impurities can creep in if racemization is not tightly controlled, so every stage of production—starting material isolation, Boc protection, workups, and drying—goes under close supervision. We go beyond standard methods to keep optical purity high, which keeps downstream sequences from forming unwanted diastereomers or incomplete chains. Our repeat analyses demonstrate consistent chiral HPLC readings above 99% enantiomeric excess. This matters to us since trace epimers can jeopardize bioactivity or regulatory compliance, especially in therapeutic peptide manufacturing.
Boc-L-Asp-OH is not just a chemical code. Its composition, solubility, and reactivity set the stage for downstream reactions. Our standard bulk supply comes as a white to off-white crystalline powder. Moisture content stays below 0.5% based on Karl Fischer analysis, as even minor hydration can change solubility in common peptide solvents. Each lot achieves a purity above 99% by HPLC, as excess byproducts or unreacted Boc anhydride complicate peptide purification and erode overall yield. Water content, DCM residue, and any sign of cross-contamination receive scrutiny in our QC rounds.
As manufacturers, we’ve field-tested our product in reactions ranging from gram-scale research to multi-kilo commercial syntheses. Chemists often comment that our Boc-L-Asp-OH dissolves evenly in DMF, DMSO, and NMP, making it easier to load on resin or in solution-phase protocols. Material that dissolves smoothly at working concentrations—without leaving sticky residues—saves time, solvents, and nerves. Clumping, dust, or unmanageable static can hint at dryness imbalances or heterogeneity. Addressing these comes from practical lessons: gentle milling, low-temperature storage, and controlled-atmosphere packaging, not just smart chemistry.
Many peptide chemists ask why they should use Boc-L-Asp-OH instead of unprotected aspartic acid or other protected forms. The answer comes from repeated bench testing and production runs. The Boc group offers lability under mild acid catalysis, which means it leaves the molecule cleanly when treated with agents like TFA or HCl, unlike some alternative protecting groups. After deprotection, the resulting L-aspartic acid couples cleanly, avoiding side reactions or lingering fragments. This efficiency supports scale-up, where minor inefficiencies in small runs balloon into cost drains at the plant scale.
Unprotected amino acids can lead to complex mixtures, problematic cyclization, or oligomerization during early peptide coupling. By contrast, our Boc-L-Asp-OH reduces these risks, offering more predictable yields and less troubleshooting. In feedback from process chemists, this reliability beats off-the-shelf alternatives—especially when moving from kg to multi-kg production, since scale brings out hidden flaws in purity or stability.
Application-wise, Boc-L-Asp-OH serves in the assembly of a broad spectrum of peptides, from pharmaceuticals to biomedical reagents. Researchers rely on it for suppressing side-chain activity while letting the main chain extension proceed with fewer distractions. A practical example: when synthesizing peptides for GLP-1 analogues or antigenic epitopes, the aspartic acid residue must integrate smoothly with other protected amino acids. If the Boc group detaches prematurely or resists removal, entire product lines go on hold. Each hour lost to purification is both a financial and an opportunity cost. That’s why detailed in-process checks and batch documentation form part of our supply routine.
Our years in this field have shaped our approach to shelf stability and user experience. Boc-L-Asp-OH keeps best in cool, dry, light-shielded packaging—no silver bullets, just well-proven routines. We use food-grade HDPE or glass bottles with sealed inner liners to keep out moisture, since water ingress speeds up Boc cleavage. Trace base can accelerate hydrolysis, so we monitor for pH drift during storage.
A subtle but real difference comes from how we dry and grind outgoing batches. Too fast, and thermal degradation leaves behind yellow hues and smeary textures. Too slow, and solvent remains, making weights unreliable. We watch particle size closely since chemistry at production scale punishes inconsistency—fine powders vaporize, but large granules fail to dissolve. Our millers run quality checks at every shift. It’s no secret to us that most complaints around Boc-amino acids trace back to this overlooked detail. We invest in people and tools to smooth this friction point.
From a manufacturing standpoint, we choose not to blend sources or mix left-over product from earlier batches. Single-lot traceability keeps data straight, and helps spot rare anomalies fast. We support customers with technical documentation straight from our plant, not repackaged or altered by intermediaries, so any background or troubleshooting flows directly from our chemists and process engineers.
Competitors offer multiple aspartic acid derivatives. The choice between Boc-L-Asp-OH, Fmoc-L-Asp-OH, or unprotected aspartic acid typically hinges on the protecting group strategy. Boc-protected amino acids have a particular place in protocols using acid-labile protection. The Fmoc format, by contrast, works where base-labile deprotection is the norm. As a manufacturer supplying both, we see the trade-offs firsthand: Boc chemistry offers faster deprotection with TFA and less risk of racemization under boc removal compared to some Fmoc regimes.
Boc-L-Asp(OtBu)-OH also appears in peptide catalogs. This derivative features simultaneous protection of the side-chain carboxyl group (with OtBu), alongside the main Boc protection. For short peptide syntheses or routes where side-chain protection is critical, this extra barrier keeps side reactions at bay. Our direct experience shows, though, that Boc-L-Asp-OH lets users introduce free side-chain carboxylates when needed—ideal when synthesizing aspartic acid-rich motifs or post-translational mimetics. Users who want maximal flexibility favor Boc-L-Asp-OH, since it lets them sequence side-chain modifications without being locked into a tert-butyl block.
Some generic suppliers cut corners or blend in low-purity material, leading to recurring solubility problems, stubborn residual odor, or stubborn foaming during scale-up. We approach these issues head-on, using parallel process verification and open logs on each step. It is not unusual for development labs to send feedback about easier peptide chain extensions or reduced need for repeated evaporations since switching to our supply. This speaks to details like consistent drying, full reaction conversion, and zero detectable side-product in spectroscopic checks.
Our chemists keep seeing how minute changes in Boc-L-Asp-OH translate to unpredictable peptide chains. At scale, even a trace of D-aspartic acid leads to partial sequence isomerism and troublesome separation. We run regular optical rotation and chiral purity checks, investing in calibration standards and internal cross-validation. Sourcing from controlled fermentative or extraction processes up front matters more than squeezing cost at the end. Contract partners and academic groups often comment that bulk shipments retain their consistency year-over-year—a symbol of our controlled input and refusal to substitute materials mid-process.
On the physical front, storage stability pays off. Whether users store Boc-L-Asp-OH in cold-rooms or on benchtops, we design packaging to resist both short-term spikes in humidity and slower creeping moisture over time. Plant engineers sometimes alert us to caking or hardening in competitor bins. This comes down to hygroscopic drift—a problem traced to careless packaging or inconsistent drying.
As shipping distances lengthen, other issues like clumping or spontaneous decomposition appear. Small details, such as using heat-sealed inner liners and volatile-capture packets inside each drum, come from direct conversations with staff who handle daily packing. We resist the temptation to cut costs or obfuscate handling instructions. Our support documents lay out best practices directly—drawn straight from cumulative years of technical production, with photos and logs on real test runs. Third-party audits verify our stability claims each year.
Modern peptide synthesis relies as much on information as on neat powders. Over the years, we’ve learned most difficulties can be traced either to unexpected side-products or hitches in reaction cleanup—not lack of academic knowledge, but missed practical experience. We supply each Boc-L-Asp-OH shipment with analytical data that matches real plant outcomes: HPLC traces show low background, NMR matches expected chemical shifts, and FT-IR identification anchors product identity.
A fresh analyst may overlook subtle shoulders or double peaks, which more seasoned chemists spot at a glance. We offer insight on troubleshooting, drawn from our own process development: if extra peaks form during coupling, our experts probe factors like batch age, solvent choices, or temperature influences. Our willingness to adjust process parameters flows directly to customers—batch performance, solubility checks, dissolution time—all tracked in-house and fed into future production runs.
As the industry moves toward higher scrutiny and regulatory checks, we keep the support documentation tied to real process runs, not just theoretical values. Batch specifications stay transparent and update annually as we refine production and testing procedures. New environmental guidelines may shift our solvent choices or introduce additional risk checks, but our response stays rooted in practical lab data.
Shifts in regulations—whether stemming from environmental pressures, workplace safety updates, or end-user requirements—push us toward greener routes and lower residual solvents year-on-year. Boc-contaminants downstream can impact both peptide API registration and final analytical certification, so we structure each aspect of our production to minimize recurring headaches for downstream users. As more peptide manufacturers seek to reduce Class 2 solvent residues, we cycle through alternate purification, extended vacuum drying, and validated cleaning to meet tough specifications.
Feedback loops with environmental health engineers in leading biotech sites led us to scale up nitric acid quantifications and ecological risk analyses. Modern packaging demands also reflect environmental concerns. Recyclable drums, high-barrier liners, and posted environmental impact statements form part of our default shipment. Regulatory responses are not always visible in the powder; they come alive in the traceability and openness in our delivery packets. Our safety and environmental sheets reflect what came off our own lines, not theoretical minimums padded for convenience.
Teaming up with users—engineers working in controlled API plants, contract development organizations, or university labs—lets us see where paperwork and on-the-ground handling diverge. Many users have pointed out that generic intermediates off the market force them to run extra analytical runs or manual cleanups, costing time and confidence. We use these insights to update our protocols and field-facing communication.
Our production philosophy revolves around continuous process evaluation and responsiveness to end-user feedback. Because we synthesize and handle Boc-L-Asp-OH from start to finish, we get an uncensored look at where challenges and improvements rest. Plant equipment investments, staff training modules, and process modifications stem straight from root-cause evaluation. Practical data sets the path—when we see a batch of Boc-L-Asp-OH clump after a trans-continental shipment, we adjust packing and drying protocols; if a pattern of intermediate impurities surfaces, our R&D chemists test alternate workups or more rigorous purification, not quick workarounds.
As regulations evolve and the bar for analytical transparency rises, we stay open to inspection. Experience teaches us that direct, honest feedback is worth more than any blanket certificate. Chemists on the receiving end need details—how each lot performs under their own conditions, not just figures that look good on paper.
Years in chemical production have shown us that the real test of a supplier is long-term consistency and openness in troubleshooting. We never view Boc-L-Asp-OH as just another intermediate; each batch carries the quiet effort of careful sourcing, skilled handling, and the willingness to course-correct as evidence and industry needs change.
Our approach to Boc-L-Asp-OH blends hands-on chemistry with a respect for user reality. At every stage, we draw lessons from what fails in practice and what works over years of production and customer collaboration. Each kilo holds the outcome of technical improvements, staff commitment, and persistent attention to detail. We measure our own progress by how rarely users need to ask for clarifications or replacements—and by the number of repeat customers who trust our product batch after batch.
Boc-L-Asp-OH bridges scientific rigor and practical workflow. By focusing on tangible outcomes—from stability through shelf-life to predictable behavior in peptide assembly—we support the chemists, engineers, and researchers who count on each delivery. Our experience, technical insight, and direct control over production enable us to stand by Boc-L-Asp-OH as not just a reliable building block, but as a tool honed for the real demands of peptide chemistry today.