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Boc-4-Amino-D-Phenylalanine

    • Product Name Boc-4-Amino-D-Phenylalanine
    • Alias Boc-D-Phe(4-NH2)-OH
    • Einecs 617-957-6
    • 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

    844047

    Product Name Boc-4-Amino-D-Phenylalanine
    Cas Number 108245-92-9
    Molecular Formula C14H20N2O4
    Molecular Weight 280.32 g/mol
    Appearance White to off-white powder
    Purity Typically >98%
    Chemical Structure C6H5-CH2-CH(NH2)-CH(NH-Boc)-COOH, D-isomer
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Storage Temperature 2-8°C (refrigerated)
    Protecting Group Boc (tert-butyloxycarbonyl) on amino group
    Chirality D-configuration
    Application Peptide synthesis

    As an accredited Boc-4-Amino-D-Phenylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Boc-4-Amino-D-Phenylalanine is supplied in a sealed 5g amber glass vial with a tamper-evident cap, labeled for laboratory use.
    Shipping Boc-4-Amino-D-Phenylalanine is shipped in tightly sealed containers to avoid moisture and air exposure. It is typically transported at ambient or cool temperatures, packaged in compliance with chemical safety guidelines, and accompanied by a safety data sheet. Handle and store according to standard protocols for laboratory reagents.
    Storage Boc-4-Amino-D-Phenylalanine should be stored in a tightly sealed container at 2-8°C, protected from light and moisture. The storage area should be cool, dry, and well-ventilated. Avoid prolonged exposure to air and potential sources of contamination. Ensure proper labeling and compliance with standard chemical storage protocols for amino acid derivatives and protected compounds.
    Application of Boc-4-Amino-D-Phenylalanine

    Applications of Boc-4-Amino-D-Phenylalanine in Industrial Manufacturing

    Boc-4-Amino-D-Phenylalanine is a specialized protected amino acid widely used by pharmaceutical, peptide synthesis, and life science manufacturers as a key intermediate and building block. Our production process meets stringent international standards required for downstream industrial processes. The following sections describe implemented industrial application scenarios by sector.

    1. Peptide API Manufacturing for Diabetes and Oncology Therapeutics

    Many global pharmaceutical manufacturers incorporate this material as a non-standard amino acid in the solid-phase synthesis of peptide-based active pharmaceutical ingredients (APIs), especially in second-generation diabetes treatments and anti-tumor agents. It enters the protected fragment-assembly phase, enabling site-specific functionalization of custom peptides. Stringent control of stereochemistry and purity directly impacts peptide sequence fidelity, which is critical for therapeutic consistency and downstream regulatory approval.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monographs on amino acid derivatives and peptides
    • US Pharmacopeia (USP) guidelines applicable to peptide synthesis

    Typical usage ratio

    • 2–10 mol% per total amino acid content, adjusted according to peptide sequence design and desired non-natural residue incorporation

    Downstream process integration

    • Integrated in solid-phase peptide synthesis following initial resin charging and Fmoc/Boc cycling
    • Participates directly in protected coupling cycles on automated peptide synthesizers or batch reactors
    • Boc group removal and subsequent deprotection step occur prior to final peptide cleavage and purification

    Final product types

    • Synthetic glucagon-like peptide-1 (GLP-1) agonists for type 2 diabetes
    • Non-natural peptide-based cytostatics for cancer therapy
    • Peptide conjugates used in controlled-release drug delivery formulations

    2. Custom Peptidomimetic Synthesis for Biotech Research Reagents

    Biotech firms utilize this compound to introduce steric and electronic modifications in peptidomimetic libraries and protein–protein interaction inhibitors. These protected derivatives allow for structure–activity relationship (SAR) exploration by precise residue placement. They are commonly used in combinatorial library synthesis for probe development, benefiting screening campaigns in early-stage drug discovery and biological target identification.

    Industry compliance standards

    • ISO 13485 (Medical Devices – Quality Management) for reagent components
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Registration, Evaluation, and Authorization (for laboratory-scale manufacture and supply)

    Typical usage ratio

    • 1–8 mol% per oligomer sequence, set according to desired variant library diversity and target protein binding pocket

    Downstream process integration

    • Enters the combinatorial assembly during parallel synthesis protocols, directly after standard amino acid activation
    • After peptidomimetic assembly, subjected to parallel global deprotection and preparative HPLC purification

    Final product types

    • High-purity peptidomimetic libraries for drug screening programs
    • Protein–protein interaction inhibitor probes for biochemical assays
    • Affinity tags for target validation projects

    3. Diagnostic Peptide Marker Production

    Clinical diagnostics manufacturers apply this raw material for preparing specialized peptide markers, used in immunoassay kits and mass spectrometry reference standards. The protected amino acid assists in achieving precise epitope mimicry for antibodies or T cell receptors, supporting reliable biomarker detection in disease monitoring workflows.

    Industry compliance standards

    • ISO 13485:2016 (Medical Devices – Quality Management Systems)
    • IVDR (EU Regulation 2017/746 on in vitro diagnostic medical devices)
    • CLSI C24-A3 guidelines (Design and Analytical Evaluation of Immunoassays)

    Typical usage ratio

    • Typically 1–5 residues per diagnostic peptide chain, based on epitope mapping and immunogenicity requirements

    Downstream process integration

    • Deployed at the synthesis stage for site-directed peptide customization
    • Processed through automated parallel peptide synthesizers
    • Final markers purified using preparative HPLC and characterized by LC-MS

    Final product types

    • Quantitative reference peptides for mass spectrometry assays
    • Epitope-specific peptide antigens for ELISA and lateral-flow test kits
    • Synthetic calibration standards for clinical chemistry diagnostics

    4. Specialty Amino Acid Supply for Enzyme Engineering Projects

    Industrial enzyme developers incorporate Boc-4-Amino-D-Phenylalanine in site-directed mutagenesis and semi-synthetic enzyme evolution programs. It allows the rational introduction of non-canonical residues at active or binding sites, enabling fine-tuning of substrate selectivity or resistance to proteolysis. Direct use in cell-free protein synthesis or chemical ligation protocols underpins expanded enzyme functionality for industrial biocatalysis applications.

    Industry compliance standards

    • OECD Good Manufacturing Practice for Chemicals
    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • Local biosafety and genetic engineering directives, e.g., NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules

    Typical usage ratio

    • Usually 0.5–3 mol% per enzyme construct, varying with mutagenesis positions and functional assay targets

    Downstream process integration

    • Introduced at oligonucleotide-directed mutagenesis or split-intein mediated protein ligation stage
    • Supports non-natural amino acid incorporation in cell-free translation or chemoenzymatic coupling systems
    • Post-assembly, enzyme constructs undergo activity screening and QC mass spectrometry

    Final product types

    • Engineered enzymes for industrial catalysis or biosensor applications
    • Tailored protease variants with resistance to breakdown in pharmaceutical formulations
    • Non-canonical amino acid-containing proteins for structural biology and functional studies
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    Certification & Compliance
    More Introduction

    Boc-4-Amino-D-Phenylalanine: Insight From the Plant Floor

    Direct From the Chemist’s Bench: Understanding Boc-4-Amino-D-Phenylalanine

    As a manufacturer who has spent years turning raw materials into high-performance peptide intermediates, certain molecules gradually earn a reputation for reliability and practical value. Boc-4-Amino-D-Phenylalanine belongs to that club. In the chemical community, the name alone signals a specialty amino acid derivative built for modern peptide synthesis workflows. Making this compound is not just about standardizing a formula—it’s about getting the details right, lot after lot, so researchers and formulators can keep their focus on the bigger scientific goals.

    Model, Specifications, and Physical Properties

    Boc-4-Amino-D-Phenylalanine is produced under tightly monitored conditions to deliver consistent purity and predictable handling. Chemists working in peptide assembly lines instantly recognize its distinguishing features: a white to off-white powder, with a molecular formula of C14H18N2O4 and a molecular weight of 278.31 g/mol. Rigorous analytical methods like HPLC and NMR spectroscopy back up every batch, ensuring an optical purity above 99% ee, with impurity profiles logged and tracked over time. The melting point gives a reliable cue that the compound has reached its proper state; the solubility across a set of practical solvents rounds out its profile, letting end-users dissolve or suspend it without guesswork.

    What stands out is the batch-to-batch reproducibility. After shipping thousands of grams worldwide, the realities of synthesizing this derivative—blocking groups, stereochemistry, moisture control—become more than technical talking points. They shift to immediate concerns, since a shift in Boc group placement or excess racemization introduces downstream headaches for any peptide chemist. Production teams maintain in-house stocks of rigorous reference standards to keep tabs on every output. That means tighter control over the product’s reactivity, and fewer surprises for clients pushing for regulatory compliance in drug substance pipelines.

    Why Peptide Chemists Look for Boc-4-Amino-D-Phenylalanine

    Boc-4-Amino-D-Phenylalanine has found its core role as a protected D-amino acid for solid-phase and solution-phase peptide synthesis. Technicians reaching for this compound know that the Boc group shields the alpha-amino site during coupling—a feature allowing sequences to be built up stepwise without unwanted cross-reactions. The D-stereochemistry holds significance for medical researchers seeking protease-resistant motifs, which hold up in both preclinical models and industrial processing. This attribute alone determines the fate of peptide drugs battling enzymatic breakdown.

    On the commercial scale, the compound moves seamlessly from research benches into kilo-labs focused on active pharmaceutical ingredient development. Years have revealed little tolerance for impurities or inconsistent stereochemical outcomes. The reputation of a peptide building block rests on whether scientists can trust it to incorporate cleanly and behave as they intend. With regulatory agencies scrutinizing both purity and trace-level side products, the margin for error only shrinks.

    Inside the plant, the team takes pride in producing Boc-4-Amino-D-Phenylalanine that withstands the full gauntlet of inspection—both in internal labs and while navigating third-party quality audits. Each production run responds to feedback, adapting steps to reduce residual solvents, scrap early side-products, and fine-tune crystallization cycles. This compound has served as a demonstration of how decades of manufacturing experience translate into a smoother path for a customer working under tight timelines.

    The Daily Realities of Scaling Production

    While some products cruise through only sporadic demand, Boc-4-Amino-D-Phenylalanine regularly appears on desks when peptide chemistry projects scale. One challenge lies in batch scheduling. High-purity derivatives often call for dedicated reactor slots and strict cleaning validation to prevent cross-contamination. Production chemists find ways to streamline, reducing solvent changes, and recycling as much energy as possible. But ultimately, purity dictates that shortcuts have little place. Every time the team weighs and samples a batch, the goal is a lot release that exceeds published specifications—not just hits the minimum.

    Logistics teams at the plant pay attention to how the compound handles temperature shifts, light exposure, and moisture—learning from every recall or customer complaint logged over the years. All it takes is a caked drum or mismanaged humidity after a maritime shipment to ruin days of careful synthesis. As manufacturers, it’s not uncommon to invest in better packaging and updated storage protocols, going beyond regulatory requirements for peace of mind. These upgrades emerge from hard-won lessons, not just lab studies.

    The analytical chemists invest hundreds of hours verifying that each shipment matches label claims and conforms to the right physical description. In the plant’s daily business, trust hinges on the ability to send a certificate of analysis that holds up under independent scrutiny. Analytical method validation isn’t just a checkbox—it becomes a matter of company reputation, shaping whether regular clients keep coming back or move on to a more trusted supplier.

    Comparison With Other Protected Phenylalanine Derivatives

    In the crowded market of amino acid derivatives, each protective group and stereoisomer fills a specific practical role. Peptide scientists familiar with Fmoc- and Boc-protected series spot the differences straight away. Boc-4-Amino-D-Phenylalanine stands apart from its L-isomer in a concrete way: the switch in orientation flips the susceptibility to enzymatic digestion and therefore influences bioactivity. For programs focused on therapeutic peptides, these characteristics shift the properties of the final molecule, impacting biological half-life and overall performance.

    Among Boc-protected amino acids, the extra amino group at the para-position of the aromatic ring in Boc-4-Amino-D-Phenylalanine introduces versatility beyond the standard derivatives. This extra functional handle opens up routes for post-assembly modifications, giving chemists more leverage to attach dyes, labels, or other bioactive fragments. In this way, Boc-4-Amino-D-Phenylalanine serves as a real innovation node, not just another raw material. The usage frequency in combinatorial peptide libraries or custom conjugation shows that the molecule stands out for those pursuing structure-activity relationships or developing targeted delivery vehicles.

    Comparing cost structures, Boc-protected amino acids usually command a higher price than their unprotected forms due to increased synthesis steps, higher purity requirements, and more exhaustive downstream processing. The trade-off yields a compound that saves hours in complicated sequences, reduces costly rework, and shrinks project cycle times in high-throughput peptide drug screening.

    Quality Assurance: The View From Inside the Facility

    From inside the plant, quality isn’t an abstract term. It emerges through the details—tracking raw material provenance, calibrating instruments, and managing operator training. For Boc-4-Amino-D-Phenylalanine, every raw input, from the phenylalanine base material to the protective groups, undergoes full traceability. Investigation teams regularly review lot histories and equipment logs, stepping in to audit when unexpected trends arise. Recurring internal reviews keep the manufacturing process sharp, catching issues before they migrate downstream.

    Quality control teams have refined their tests to screen for not just main product content, but also for diastereomers, incomplete reactions, and byproduct profiles specific to Boc and D-phenylalanine chemistry. This attention to detail results in certificates that not only list assay figures, but describe impurity levels, chiral purity, and any relevant context, such as recent updates in test methods or special observations found during processing. Regular collaboration with independent analytical labs helps confirm results, closing the loop between in-house analysis and customer expectations.

    Any manufacturing veteran has stories of batches that almost passed, but held warning flags on further scrutiny. Such cases push the team to qualify, then requalify, all in-process controls. In the end, it’s the client and their end-user—sometimes vulnerable patients—who depend on the manufacturer catching every last outlier.

    Supporting Custom Applications and Client Collaboration

    Engagement with customers running ambitious chemistry projects consistently shapes manufacturing updates. Sometimes, a research group requests an atypical counter-ion or needs material delivered at a specific particle size. Other times, early-stage clinical developers seek stronger documentation, expanded impurity profiling, or retesting protocols to clear regulatory scrutiny for drug filings. The relationship between plant and project manager grows out of credibility: respond fast, acknowledge feedback, and innovate if established routines are holding up downstream processes.

    Commercial teams, scientists, and technical managers meet regularly to set priorities for each quarter. Feedback from recurring orders for Boc-4-Amino-D-Phenylalanine justifies investments in better isolation techniques, automated quality testing, and expanded storage infrastructure. The constant flow of communication with experienced chemists, whether it’s a reminder about handling sensitive intermediates or an urgent escalation due to an unexpected impurity, anchors the production philosophy in practicality—not just theoretical optimization.

    Meeting the Needs of Evolving Regulatory Standards

    Regulatory agencies around the world are tightening standards. For those producing Boc-4-Amino-D-Phenylalanine, adaptation becomes part of daily business. GMP compliance, electronic batch records, and method validation reports are daily realities, not conceptual checklists. Technical files capture the full manufacturing history, making traceability and quality data available for auditors, clients, and regulatory authorities. Filing updated DMFs or supporting customer submissions means the plant not only makes the molecules—it keeps the documentary backbone for approval.

    From a manufacturer’s perspective, the regulatory environment drives transparency. Every audit—internal or third-party—yields valuable lessons. Investments in new purification technologies or advanced automation arise from hard feedback, learning where last year’s quality controls left gaps. The priority stays clear: if Boc-4-Amino-D-Phenylalanine is destined for clinical research or commercial markets, compliance and full disclosure follow each bottle out the door. Errors cost more than rework or waste; they risk both client and patient safety. That pressure sharpens commitment to best practices.

    Solving Real-World Challenges in Amino Acid Synthesis

    Manufacturing Boc-4-Amino-D-Phenylalanine means navigating the practical realities of specialty chemical synthesis. Reproducibility of chiral centers, minimization of hazardous byproducts, and waste stream management hold constant importance. Everyone from the reactor operators to the quality assurance specialists know that even a slight deviation in solvent grade or reactor temperature could mean a run is scrapped, not salvaged.

    Response to market demands sometimes challenges the process design. Surges in peptide drug development push for higher output, and that increases the strain on every logistics and production element. The team responds by introducing more robust process analytical technology, stepping up automation, and cross-training personnel. Waste minimization strategies get added benefit, with solvent recycling systems and byproduct repurposing becoming both regulatory and financial priorities.

    Long-term, the goal is sustainable growth. Blending decades of synthetic chemistry know-how with modern manufacturing builds momentum toward lower waste, higher throughput, and safer work environments. Each successful batch feeds back into process improvement—every learning moment in the plant becomes a potential gain for the next lot.

    Lessons Learned and Looking Forward

    Years spent making Boc-4-Amino-D-Phenylalanine have underscored that reliability and deep knowledge define real manufacturing. Unlike resellers and traders, the plant stakes its reputation on intimate understanding—how each step in the synthesis, each quality test, and every shipping event affects a researcher’s outcomes. The compound has carved out its niche in workflows where purity, performance, and reproducibility shape the entire success of a project. When new challenges arise—faster delivery, tighter analytical tolerances, custom specifications—a history of open dialogue and investment in technology turns today’s pain points into tomorrow’s achievements.

    Making Boc-4-Amino-D-Phenylalanine isn’t just about a catalog entry; it’s about finding the sweet spot between tradition and continuous improvement. For every scientist assembling a new peptide, for every customer pushing the limits of what’s possible in pharmaceutical development, the commitment stays the same: send out only what the team would trust in their own work. This approach, tested in laboratories and refined on the plant floor, continues to set the benchmark for specialty amino acid manufacturing.