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N-Boc-Beta-Phenyl-D-Phenylalaninol

    • Product Name N-Boc-Beta-Phenyl-D-Phenylalaninol
    • Alias Boc-D-Ph2alol
    • Einecs 820-736-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    669855

    Product Name N-Boc-Beta-Phenyl-D-Phenylalaninol
    Cas Number 124605-04-3
    Molecular Formula C20H25NO3
    Molecular Weight 327.42 g/mol
    Appearance White to off-white solid
    Purity Typically >98%
    Melting Point 82-85°C
    Solubility Soluble in ethanol, dichloromethane, methanol
    Optical Rotation [α]D +20° to +25° (c=1, CHCl3)
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Synonyms Boc-D-β-phenylphenylalaninol, (R)-N-(tert-Butoxycarbonyl)-β-phenylphenylalaninol
    Smiles CC(C)(C)OC(=O)N[C@H](Cc1ccccc1)C(O)c2ccccc2
    Inchi InChI=1S/C20H25NO3/c1-20(2,3)24-19(23)21-17(14-15-8-4-6-9-16(15)12-17)18(22)13-10-5-7-11-13/h4-11,14,17-18,22H,12-13H2,1-3H3,(H,21,23)/t17-,18-/m1/s1
    Chiral Purity Typically >99% ee

    As an accredited N-Boc-Beta-Phenyl-D-Phenylalaninol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing N-Boc-Beta-Phenyl-D-Phenylalaninol, 5g, sealed in an amber glass bottle with tamper-evident cap, labeled with safety information.
    Shipping N-Boc-Beta-Phenyl-D-Phenylalaninol is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Packaging complies with applicable regulations for safe transport of laboratory chemicals. It is handled as a non-hazardous solid, but shipping may require documentation due to its specialized use. Temperature and stability are monitored as recommended.
    Storage N-Boc-Beta-Phenyl-D-Phenylalaninol should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. The recommended storage temperature is 2–8°C (refrigerator). Avoid exposure to strong acids, bases, and oxidizing agents. Ensure proper labeling and follow standard laboratory safety protocols to prevent contamination and decomposition.
    Application of N-Boc-Beta-Phenyl-D-Phenylalaninol

    Applications of N-Boc-Beta-Phenyl-D-Phenylalaninol in Industrial Manufacturing

    As a direct manufacturer of N-Boc-Beta-Phenyl-D-Phenylalaninol, we provide consistent quality for integration into advanced downstream sectors. Its unique chiral and protected amino alcohol structure supports specialized synthesis routes in regulated industries. Below we outline proven commercial application scenarios, each with focused technical context, compliance factors, and typical downstream integration approaches.

    1. Chiral Intermediate Sourcing for Active Pharmaceutical Ingredients (APIs)

    Many pharmaceutical manufacturers select this compound as a key chiral intermediate during the multistep synthesis of non-racemic active molecules, especially in the development of beta-phenyl-substituted compounds or as a pivotal building block in the preparation of D-isomer selective therapeutic agents. Due to strict regulatory submissions and batch traceability, the incoming quality of this intermediate directly affects downstream API stereo-purity and enables precise chiral control during solid or liquid phase peptide assembly under GMP conditions.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • USP/NF and EP monograph traceability (where relevant to custom synthesis clients)
    • FDA drug master file (DMF) supporting documentation for supplied lots
    • 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.1 to 0.8 molar equivalents per target API batch, adjusted based on targeted enantiopurity and process mass intensity (PMI)

    Downstream process integration

    • Charged during enantiospecific condensation or reductive amination step after deprotection
    • Stage-specific chromatography and in-process HPLC chiral analysis
    • Intermediate isolation and purification prior to conversion to final API salt or ester

    Final product types

    • Non-racemic APIs (for CNS, oncology, or cardiovascular treatments)
    • Advanced chiral pharmaceutical intermediates
    • Enantiopure beta-amino alcohol derivatives

    2. Custom Peptide Synthesis Reagent Supply

    Specialized peptide research and cGMP manufacturing facilities utilize this compound as a protected amino alcohol during the solid-phase or solution-phase synthesis of modified peptide chains. Its N-Boc group protects the amine functionality, affording site-selective coupling and smooth elongation on automated synthesizers. Deprotection prior to final fragment assembly ensures minimal racemization risk, with thorough impurity control driven by peptide purity demands for regulatory approval.

    Industry compliance standards

    • ISO 9001:2015 certified QMS for custom peptide synthesis
    • ISO 13485 for medical peptide products
    • GMP for clinical grade peptides (FDA 21 CFR 210/211)
    • Synthetic peptide guideline specifications (ICH Q6B)

    Typical usage ratio

    • One equivalent per residue for manual SPPS; adjusted to 0.9–1.2 equivalents based on the specific synthesizer configuration

    Downstream process integration

    • Charged during amino acid coupling cycles in Fmoc/tBu or Boc/Bzl-based synthetic workflows
    • Deprotected via TFA cleavage step prior to C-terminal modifications
    • QC by UPLC-MS after integration and final cleavage

    Final product types

    • Synthetic peptide-based drug candidates
    • Diagnostic peptides and peptide libraries
    • Specialty peptide derivatives for research or in vitro use

    3. Advanced Intermediate for Chiral Ligand Synthesis in Asymmetric Catalysis

    Catalyst manufacturers employ N-Boc-protected beta-phenyl amino alcohols for ligand construction in metal-catalyzed asymmetric reactions. As a versatile chiral backbone, it facilitates enantioselective ligand frameworks for transition metal complexes. Consistent supply of high-purity material enables formulation of specialty ligands that control enantioselectivity in high-throughput catalytic manufacturing, directly supporting process patent portfolios for downstream partners.

    Industry compliance standards

    • REACH Annex VII–X compliant registration for specialty chemicals
    • ISO 17025 traceable documentation of compound identity and purity
    • Internal GMP-like protocols for ligand precursor handling
    • Hazardous waste documentation (as per local authority for metal–organic residues)

    Typical usage ratio

    • 0.2 to 1.5 molar equivalents within custom ligand synthesis pathways, varied with desired catalyst stereochemistry and ligand loading on metal centers

    Downstream process integration

    • Inserted post-metalation step when forming optically active ligand–metal complexes
    • Protection group removal coordinated with metal center compatibility checks
    • Ligand functionalization performed under anhydrous, inert atmosphere

    Final product types

    • Chiral ligands for asymmetric catalysis in fine chemical synthesis
    • Enantioselective catalyst components for industrial processes (e.g. hydrogenation, epoxidation)
    • Specialty metal–ligand complexes for process R&D

    4. Intermediate for Small Molecule Research Compound Libraries

    Contract research organizations and pharmaceutical discovery labs select N-Boc-beta-phenyl-D-phenylalaninol as an advanced building block for combinatorial chemistry. Its stereo-defined backbone and Boc-protected amine support incorporation into diverse chemical scaffolds, allowing rapid parallel synthesis and SAR (structure–activity relationship) exploration under compound library generation workflows. Rigorous QC protocols enable consistent structure assignment for each sample.

    Industry compliance standards

    • ISO 9001:2015 for compound library production
    • GLP (OECD Good Laboratory Practice) for traceability in screening applications
    • Controlled substance exclusion (US DEA, EMEA as relevant to research jurisdiction)
    • Hazardous chemical labeling (GHS/CLP compliance for exports)

    Typical usage ratio

    • 0.05–0.2 mmol per 1.0 mmol scaffold, optimized for parallel synthesis protocols and diversity-oriented synthesis

    Downstream process integration

    • Employed as a variable-position building block in split-and-pool or sequential addition routes
    • Applied post-core scaffold assembly for late-stage diversification
    • QC performed via LC-MS and NMR for each library member

    Final product types

    • Diverse research compound libraries
    • Screening sets for medicinal chemistry programs
    • Reference samples for SAR and lead validation
    Free Quote

    Competitive N-Boc-Beta-Phenyl-D-Phenylalaninol 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 sales7@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    N-Boc-Beta-Phenyl-D-Phenylalaninol: A Practical Approach to Precision in Amino Alcohol Synthesis

    Insight from the Production Floor

    N-Boc-beta-Phenyl-D-phenylalaninol is a chemical that bridges laboratory demands with scalable industrial aims. Built around a backbone many research chemists recognize, this compound draws attention due to its role in customizing peptidic, pharmaceutical, and specialty chemical projects. Over the years, our team has handled hundreds of custom orders, small batch requests, and routine ton-scale runs involving this product. A down-to-earth look at this molecule reveals its value goes deeper than a catalog entry.

    This molecule carries both the N-tert-butoxycarbonyl (Boc) protecting group and the chiral beta-phenyl moiety derived from D-phenylalanine. We produce it under strict handling and isolation conditions to preserve enantiomeric purity, which often determines the ultimate outcome in enzyme inhibitors, advanced intermediates, and asymmetric catalysis projects.

    In a manufacturing environment, chiral starting materials separate good science from guesswork in drug discovery. Once we introduced N-Boc-beta-Phenyl-D-phenylalaninol into our production line, we noticed reduced waste in parallel syntheses and better consistency along downstream reaction steps. Peptide researchers in the market often mention that unchecked impurities complicate purification challenges. Before scaling up, we addressed this with advanced chiral column analysis and in-line monitoring. The result ensures a product that not only hits expected chiral specs but also avoids off-purity pitfalls that frustrate downstream users.

    Specifications That Translate to Real Benefits

    Every lot undergoes close scrutiny before it leaves the reactor. The white, crystalline solid usually appears with measured melting points and carries batch-specific enantiopurity data. For the best outcomes in chiral pool synthesis or prodrug research, we've learned batch-to-batch reproducibility matters as much as purity itself. Chiral HPLC serves as our main watchdog, frequently paired with mass spectrometry and proton NMR profiling so every order speaks for itself. Customers working under GMP or with regulatory submissions seem to appreciate documentation that covers trace components and their mitigation.

    Historically, the Boc group serves as a reliable safeguard against overreactions in multistep synthesis. In our operations, controlled deprotection steps save our clients hours of troubleshooting, particularly during scale-up. Boc gives a practical balance between stability during storage and lability under the right acidolytic conditions. For N-Boc-beta-Phenyl-D-phenylalaninol, both the selection of protecting groups and highly selective synthetic shortcuts grew out of collaborations with chemists looking for scalable, predictable intermediates. It's never just about making grams – it’s about making material that performs.

    Where Performance Meets Versatility

    Pharmaceutical companies and custom research labs use this compound to unlock new peptidomimetic analogs and beta-amino derivatives. Many of our partners design bioactive molecules that exploit the unique conformation imparted by the beta-phenyl and D-configuration. In early days, some reported purification headaches due to close-boiling impurities. We solved that by introducing staged crystallization and multi-stage filtration tailored specifically to this compound’s solubility behavior. This reduced side-product formation during hydrogenation and allowed safer, more predictable transitions into subsequent coupling steps.

    Research teams frequently use N-Boc-beta-Phenyl-D-phenylalaninol as a key building block. Its chiral alcohol handle opens routes to secondary modifications, including selective oxidation and amide formation. Medicinal chemists who chase new scaffolds for CNS-active compounds come back to this substrate because it provides both flexibility and precision. Our feedback loop from scale-up runs has shown that tight control over residual solvents and particle size distribution minimizes downstream processing loss, particularly in pilot plant settings.

    How This Product Stands Apart

    Not all chiral intermediates deliver cleanly on their promises. Some lack robust documentation, others fall short when scaled above bench-level batches. Our long-term engagement with the product starts from raw material selection, moves through reaction design, and ends at rigorous purification and final packing under climate-controlled conditions. Occasionally, we receive feedback about carry-over contaminants from upstream syntheses. Tweaking temperature profiles and washing protocols made a real difference in high-throughput production.

    Compared to similar compounds – say, the L-enantiomer or the free amino alcohol without Boc – N-Boc-beta-Phenyl-D-phenylalaninol holds its own because of stereochemical integrity. Users in the polymer and agrochemical fields sometimes probe these differences since racemization in non-specific routes ruins entire synthesis campaigns. That’s why keeping an eye out for D:L ratios pays off in both research and commercial-scale processing. The added Boc group adds storage stability, a practical concern for those who order several kilograms at a time.

    Competitors sometimes source from traders, whose suppliers change batch-to-batch and region-to-region. By maintaining synthesis in-house and controlling the quality from the ground up, we notice fewer surprises in both process chemistry and final product applications. Over time, this leads to fewer customer returns and better relationships with chemists who place a premium on transparency. Recognizing real costs at each step—from chiral precursors to solvent recovery—helps us keep our product dependable.

    Addressing Real-World Process Challenges

    A few years back, a customer developing a peptide active ingredient flagged inconsistent coupling yields. After some digging, we found trace water content crept in during extended storage. Our solution: upgraded desiccant protocols and vacuum sealing post-packaging. Since then, similar complaints vanished. Sometimes the simplest fixes solve stubborn problems but only if the manufacturer tracks the full story from raw material through delivered drum.

    Handling N-Boc-beta-Phenyl-D-phenylalaninol on a plant floor means training operators to spot signs of over-grinding or abrasion during transfer. While it behaves well under typical lab conditions, industrial transfer lines present new risks for dust formation or clumping. We tackled this by recalibrating dryer cycles and switching to anti-static bins, minimizing agglomeration issues in downstream blending operations.

    The knowledge we gain from commercial campaigns shapes the next round of improvements. Chemists on pilot campaigns often suggest tweaks—smaller mesh screenings, altered solvent choices, or revised deprotection profiles. Taking this feedback seriously helps us tune our process, optimize delivery timelines, and meet shifting regulatory documentation requirements with accuracy.

    Safety, Consistency, and Environmental Responsibility

    With increasing attention on supply chain reliability and safety, chemical plants like ours face scrutiny from regulators and customers alike. From batch records to material traceability, we practice deep documentation at every step. Our experience tells us that the best results come from full transparency: regular internal audits, detailed impurity logs, and chain of custody tracking.

    Responsible waste handling remains critical. We keep solvent recycling rates high and minimize hazardous by-products using green chemistry wherever we can. N-Boc-beta-Phenyl-D-phenylalaninol production generates minimal process waste thanks to continuous improvement. Measures such as updated reaction vessels, high-yield purification cycles, and reusable filtration media all contribute to environmentally sound outcomes. Engineers at our site continuously scout for milder reagents and less energy-intensive steps, driving both efficiency and lowered risks for our workforce.

    From time to time, regulatory guidance shifts, especially around residual solvent levels and chiral purity standards. Direct input from pharmacologists and compliance analysts lets us anticipate these developments and adjust protocols before bottlenecks appear. Many end-users report passing audits and internal QHSE testing more easily after switching to our material, which reflects the discipline built into our production and documentation procedures.

    Supporting Industry Innovation

    Novel therapeutics, high-performance enzymes, and tailored specialty polymers all need reliable sources of chiral building blocks. Our regular production campaigns for N-Boc-beta-Phenyl-D-phenylalaninol support customers reaching deep into uncharted chemical territory. It’s not unusual to hear from researchers who use our compound to streamline synthesis of fragments for SAR libraries, pharmaceutical intermediates, or even advanced ligands in catalytic research.

    Chemical innovation rarely happens in a vacuum. Collaborating closely with end-users provides the insights required for steady improvement. At our facility, on-site analytical teams frequently engage with clients in real time, troubleshooting issues with reactivity, shelf life, or documentation. Sometimes, this means reworking an order to tighter specs. More often, it means refining isolation protocols to keep up with shifting downstream needs. Over time, this shared desire for technical problem-solving strengthens the relationship between manufacturer and researcher.

    Many academic groups and pharmaceutical developers seek out niche chiral molecules in small to medium quantities, which presents a different set of challenges than commodity-scale batches. Our investment in modular reactors, flexible production lines, and dedicated crystallization equipment brings much-needed agility. We see firsthand how rapid campaign switching and custom batch sizes empower our customers to take meaningful risks in their work.

    Feedback and Continuous Improvement

    Engaging directly with leading researchers keeps us honest about what works and what falls short. Solvent compatibility in scaling-up, safer container design, or just-in-time delivery—all these concerns surface during regular project debriefs. Most improvements in our plant came from listening to chemists at the bench, not top-down management mandates.

    Once, an order destined for an international client ran into unexpected customs delays related to documentation lapses on certain trace component profiles. Our team adjusted shipping protocols and now maintains a standardized set of batch analytical data to go with every shipment, smoothing out potential choke points before they become real bottlenecks. Such experiences reaffirm the benefit of close integration between technical, production, and logistics teams.

    Occasionally, we hear requests for alternative protecting groups or lighter environmental footprints. These drive our process development chemists to test new reagents, shorter synthesis routes, and optimized workups that use fewer resources. It’s this responsive spirit—born from the practical realities of the synthesis bench and the needs of the user—that gives our product its staying power.

    Why Long-Term Users Stick With Us

    Firms that value reliability and open communication tend to become long-standing partners. Tighten the spec, increase chiral purity, speed up turnaround—every year, requirements evolve, but the basics of trust remain. By staying present in the conversation, we learn what features to refine and where to deliver extra value.

    Experienced chemists know that a poorly characterized or inconsistent reagent disrupts costly syntheses, introduces uncertainty, and wastes resources. Our focused approach—control over every production phase, live analytical feedback, fast response to improvement suggestions—sets a higher bar for what a chemical supplier can offer. This makes a practical difference when projects run on tight deadlines or when rare reagents command critical roles in scale-up plants.

    Some customers request custom packaging, tailored dryness standards, or strict inert-atmosphere shipping. By keeping warehousing and packaging on-site, we implement these requests without added delays. The attention to detail built into each order reduces emergency interventions and keeps project timelines on track.

    Looking Ahead

    Chemical manufacturing never stands still. Step-by-step updates to our purification protocols, investments in new analytical tech, and outreach to regulatory advisors have helped us stay current with changing industry standards. Bringing new synthesis ideas from bench to bulk requires both scientific rigor and responsiveness to feedback from the field. Our journey with N-Boc-beta-Phenyl-D-phenylalaninol reflects this blend of careful planning and openness to adjustment.

    As downstream innovations accelerate in fine chemicals, peptides, and broader custom synthesis, users expect not just a reagent, but a partner that can flexibly address their evolving needs. We plan to keep expanding our capacity, improve documentation systems, and work with leading academic and industry voices to refine both the product and its support infrastructure.

    N-Boc-beta-Phenyl-D-phenylalaninol, from synthesis to shipment, showcases the tangible results of open communication, careful quality management, and persistent attention to user feedback. The experiences gathered from each campaign culminate in a product that serves real-world synthesis without cutting corners. We look forward to supporting the next generation of chemical and pharmaceutical progress using this versatile tool, built from the collective wisdom of our production and research partners.