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Boc-D-Bpa-OH

    • Product Name Boc-D-Bpa-OH
    • Alias Boc-D-4-Benzoylphenylalanine
    • Einecs 837-730-7
    • 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

    741466

    Product Name Boc-D-Bpa-OH
    Chemical Name tert-Butoxycarbonyl-D-benzoylphenylalanine
    Molecular Formula C22H25NO5
    Appearance white to off-white solid
    Cas Number 116683-65-7
    Purity ≥98%
    Storage Temperature 2-8°C
    Solubility soluble in DMSO, slightly soluble in methanol
    Optical Activity [α]20/D -40° (c=1, DMF)

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

    Packing & Storage
    Packing Boc-D-Bpa-OH is packaged in a 1 gram amber glass vial, sealed with a screw cap and labeled for laboratory use.
    Shipping **Boc-D-Bpa-OH** is typically shipped at ambient temperature, protected from moisture and light, in tightly sealed containers. The packaging ensures chemical integrity and safe handling, in compliance with standard shipping regulations for research chemicals. Expedite shipping is recommended to minimize product degradation and maintain optimal quality upon arrival.
    Storage **Boc-D-Bpa-OH** should be stored in a tightly sealed container under cool, dry conditions, ideally at 2–8°C (refrigerator). Protect it from light and moisture to prevent decomposition of the Boc protecting group and maintain its chemical stability. Avoid exposure to strong acids or bases and sources of ignition. Handle under inert atmosphere if long-term storage is required.
    Application of Boc-D-Bpa-OH

    Applications of Boc-D-Bpa-OH in Industrial Manufacturing

    Boc-D-Bpa-OH serves as a high-purity amino acid intermediate, valued for its protective group stability and enantiomeric precision, supporting advanced peptide and pharmaceutical synthesis workflows across regulated manufacturing environments. Below, we detail several core application sectors where our production expertise matches stringent downstream customer requirements.

    1. GMP Peptide API Synthesis

    Our material meets rigorous peptide synthesis demands in the pharmaceutical sector, where manufacturers integrate Boc-D-Bpa-OH during classic solution-phase or automated solid-phase peptide synthesis (SPPS). Its use enables precise chiral incorporation for therapeutic peptide APIs, supporting high-yield linear chains with minimized racemization and clean post-synthetic deprotection steps. Critical applications involve dosage form actives for hormonal therapies and targeted oncology agents.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP <1790> Peptide Synthesis
    • Ph. Eur. 2.9.40 Amino Acid Analysis
    • FDA 21 CFR Part 210/211

    Typical usage ratio

    • Standard 1:1 stoichiometry relative to target sequence position; in solid-phase peptide synthesis, 10-20% molar excess over resin loading to ensure full coupling, adjusted for resin type and scale.

    Downstream process integration

    • Incorporated during the chain elongation phase of SPPS workflows, followed by TFA-mediated Boc group removal and subsequent fragment condensation or side-chain modifications.

    Final product types

    • Injectable peptide pharmaceuticals
    • Oral peptide drugs
    • Peptide-based diagnostic imaging agents
    • Custom-length research-grade peptides

    2. Diagnostic Peptide Substrate Production

    Diagnostic kit manufacturers rely on Boc-D-Bpa-OH to synthesize specific fluorogenic and chromogenic substrates used for laboratory enzyme assays and medical imaging probes. Its structural features allow controlled insertion of benzoylphenylalanine residues, improving substrate stability and signal intensity across automated detection platforms targeting protease activity profiling.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices QMS
    • CLSI C31-A for Enzyme Substrate Manufacturing
    • EU In Vitro Diagnostic Regulation (IVDR) 2017/746
    • EN ISO 14971 Risk Management for Medical Devices

    Typical usage ratio

    • Formulators dose Boc-D-Bpa-OH at a 1:1 equivalence to the corresponding residue sites; 1.2–1.5x excess applied for high-throughput solid-phase batch synthesis to achieve complete conversion and reduce failure rates.

    Downstream process integration

    • Introduced during resin-bound peptide sequence assembly, particularly for optical probe construction, followed by cleavage, purification via HPLC, and occlusion synthesis for diagnostic kit integration.

    Final product types

    • Enzyme assay substrates (e.g., trypsin, chymotrypsin)
    • FRET-based imaging reagents
    • Synthetic peptide standards for medical labs
    • ELISA controls and substrates

    3. Custom Antibody Epitope Synthesis

    Biopharmaceutical and research reagent manufacturers use Boc-D-Bpa-OH in custom peptide antigen production, enabling synthesis of rare and site-specific epitopes required for monoclonal antibody development. The compound’s structural integrity ensures recognition motifs closely mimic target proteins, which enhances the selectivity and reproducibility of downstream immune response studies or biologic therapeutic development.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • OECD Principles of Good Laboratory Practice (GLP)
    • AAALAC Guidelines (if used for in vivo validation)
    • USDA Animal Welfare Act (for immunization protocols)

    Typical usage ratio

    • Stoichiometric parity with the targeted sequence residue, with up to 1.3-fold excess for longer epitope chains to compensate coupling efficiency decline in later elongation cycles.

    Downstream process integration

    • Applied during manual or automated chain assembly steps, generally after initial strategy design for sequence-specific peptide antigens, followed by cleavage and cyclization or conjugation to carrier proteins.

    Final product types

    • Custom immunogen peptides
    • Epitope mapping standards
    • Biotinylated peptides for affinity assays
    • Antibody production kits

    4. Photoreactive Peptide Mapping and Cross-Linking Studies

    Researchers and biotechnology firms employ Boc-D-Bpa-OH to introduce photoreactive residues in synthetic peptides intended for protein–protein interaction mapping and cross-linking mass spectrometry. The benzoyl moiety supports covalent binding upon UV activation, which stabilizes transient complexes and facilitates reproducible characterization in structural biology.

    Industry compliance standards

    • NIH Recombinant DNA Research Guidelines
    • MS/MS Peptide Cross-Linking Best Practices (ASMS 2025)
    • Institutional Biosafety Committee (IBC) Oversight
    • ISO/IEC 17025:2017 Calibration and Testing Laboratories

    Typical usage ratio

    • Selected at a 1:1 ratio with insertion site, with 5–10% excess to overcome photo-induced degradation during parallel synthesis batches; final ratio tailored to the desired cross-linking density in protein mapping experiments.

    Downstream process integration

    • Integrated at designated positions during solid-phase peptide synthesis, typically prior to final deprotection and labeling, immediately followed by photoirradiation and sample preparation for analytical mass spectrometry.

    Final product types

    • Photoreactive cross-linking peptides
    • Peptide probes for structural biology
    • Protein–protein interaction mapping kits
    • Custom mass spectrometry standards
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    Competitive Boc-D-Bpa-OH 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 admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    Boc-D-Bpa-OH: A Reliable Building Block for Modern Peptide Synthesis

    Understanding Boc-D-Bpa-OH in Our Production

    Over the years, our team has focused on high-purity amino acid derivatives that streamline peptide synthesis and satisfy strict research and industrial demands. Boc-D-Bpa-OH stands out as a protected aromatic amino acid, recognized for its performance in solid-phase and solution-phase peptide assembly. This specialty product features the tert-butyloxycarbonyl (Boc) group attached to the alpha-amino function of D-4-benzoylphenylalanine, protecting the reactivity of the alpha-amino group during multi-step synthesis. This design reduces unwanted byproduct formation and simplifies deprotection procedures during peptide chain elongation. Our chemists use precise control over raw materials, environmental parameters, and purification steps to ensure that each batch meets stringent standards.

    Product Model and Specifications Informed by Our Experience

    Several technical features define Boc-D-Bpa-OH as we manufacture it. Most notable is its fine, free-flowing powder form and exceptional solubility characteristics in polar organic solvents relevant to peptide work, such as DMF and DCM. Each production run maintains strict limits on water content, residual solvents, and heavy metal traces to avoid disruptions in downstream synthesis or reactions with sensitive reagents like coupling agents (e.g., HATU, DIC, or PyBOP).

    From our production floor, we see demand for both research-scale and kilogram quantities. This variability shapes our batch size flexibility, ranging from small lots for academic users to larger, reproducible batches destined for pharmaceutical labs. Every kg goes through multi-step crystallization and chromatography, with QC validated by HPLC purity over 98% and precise rotation and melting point checks. Our analytical team checks each lot's identity using detailed NMR and mass spectrometry, which helps users trace any synthesis challenge back to the starting building block, streamlining troubleshooting and method optimization.

    Applications in Peptide and Protein Development

    Each year, the requirements of pharmaceutical and biotechnology customers push our production processes forward. Boc-D-Bpa-OH acts as a photoreactive crosslinker when researchers incorporate it into synthetic peptides and proteins. Since D-4-benzoylphenylalanine contains a benzophenone group, it offers selective covalent bond formation upon UV irradiation, often used to study protein-ligand or protein-protein interactions. The ability to position the crosslinking site precisely within peptide sequences allows for high-resolution mapping of molecular interactions, valuable in protein engineering, ligand-receptor identification, and even drug discovery programs.

    Beyond basic research, some projects focus on developing photoaffinity labels for membrane-bound receptors, GPCRs, and enzymes. Our formulation of Boc-D-Bpa-OH makes it possible to build protected peptide segments without unintended side reactions, minimizing time spent troubleshooting obscure cleavage or cross-reactivity during deprotection. The D-configuration grants resistance to proteolytic degradation when engineers need metabolic stability in peptide analogs. Medicinal chemists often request this stability for in vitro and in vivo work, aiming to expand peptide drug half-life or study D-amino acid incorporation impacts.

    Users also tap into this intermediate to build custom probe libraries for target identification, structure-activity relationship (SAR) studies, and chemical biology research. The product fits well into both solution-based and automated synthesizers due to its reliable physical properties and high batch-to-batch reproducibility. As production staff, we continually optimize to reduce trace contaminants, which could otherwise cause delays in complex, multi-step syntheses or force expensive peptide purification cycles downstream.

    Distinctions Compared to Other Peptide Building Blocks

    Feedback from our long-term partners often focuses on the challenges of synthesizing peptides with non-standard amino acids. Boc-D-Bpa-OH brings a unique photoreactive benzophenone side chain, a feature rarely matched by more common aromatic amino acids like Boc-phenylalanine or Boc-tyrosine. The ability to induce crosslinking under mild conditions, without side-chain oxidation or decomposition, gives Boc-D-Bpa-OH a distinct edge for downstream structure probing.

    Compared with common Fmoc-protected versions, our Boc series appeals to those using Boc-chemistry protocols, especially in peptide segments that require strong acid deprotection steps. Some synthesis projects struggle with side-product formation due to incomplete Boc removal. Our process consistently produces a product with minimal scavenger-demanding byproducts, so users often report smoother cleavage and final peptide purification. Even on industrial scales, consistency remains a hallmark.

    For users contemplating the shift from standard amino acids, the D-configuration in Boc-D-Bpa-OH supplies two-fold value: resistance to enzymatic digestion and altered conformational propensity in the peptide backbone. This opens routes for engineering peptides with higher biological stability, or for examining structure-activity dependencies in pharmaceutical research.

    From a practical perspective, comparison with Fmoc-D-Bpa-OH finds lab teams choosing our Boc form for its compatibility with certain resin handles or acid-stable protecting group strategies. Our technical team fields questions about switching between Fmoc and Boc chemistry almost daily. The decision rests on synthesis workflow compatibility, deprotection conditions, or integration with existing peptide assembly methods. We guide customers through the trade-offs based on our process knowledge and real-world application feedback.

    Occasionally, partners require analytical or regulatory documentation alongside supplies. Our documentation includes full analytical data, impurity profiles, and supplementary technical notes, all generated in-house as part of every batch’s release. Without these robust controls, batch variation or contaminant risk would stall or invalidate high-value peptide syntheses. Direct feedback from process chemists and peptide engineers feeds into our continual improvement cycle.

    Ensuring Quality and Supply Chain Stability

    Our experience highlights a basic principle: high-value peptide building blocks are only as useful as their reliability. We have seen how a contaminated amino acid source can delay entire drug development projects or invalidate assay results. Consistency begins with high-quality raw materials and continues with rigorous process controls. We source and test starting amino acids, protectants, and solvents on a lot-by-lot basis, tracking every supplier’s past quality record and making adjustments as soon as any deviation arises.

    Our scale-up and purification technology uses equipment reserved solely for non-proteinogenic, photoreactive amino acids. This prevents even trace cross-contamination, a factor sometimes overlooked by less specialized facilities and a cause of synthesis failures at the peptide elongation or deprotection steps. In our plant, continuous training and strict environmental monitoring keep particulate and moisture contamination below levels that could impact the reproducibility of solid-phase syntheses.

    Quality checks extend beyond the production line. Each container ships only after full certification of analysis. Our technical support regularly collaborates with users to tailor batch sizes and custom lot controls, which prove vital for GMP-related projects or regulatory submissions. Many larger manufacturers ship amino acid derivatives without full supporting documentation, but we invest resources in analytical traceability because we have seen the consequences of skipping this investment: failed syntheses, lost time, and budget overruns.

    A robust supply chain also means predictable lead times. Our strategy uses co-located raw material stores and vertical integration of key synthetic steps, limiting exposure to transport delays or geopolitical risks that affect other global chemical suppliers. Our team monitors long-term demand trends and builds inventory buffers for forecasted research cycles. Thanks to these measures, users repeatedly report minimal downtime in their peptide development programs.

    Technical Support and User Collaboration

    Beyond supplying Boc-D-Bpa-OH, we maintain close ties with researchers and production teams. Our chemists answer technical questions daily, drawing on personal experience, in-process troubleshooting, and a database of peptide synthesis case studies. Sometimes, users encounter unusual solubility, side-reaction risks, or unexpected byproducts in their own labs. Other times, a workflow calls for custom packaging, extra drying steps, or documentation for regulatory filings. We see firsthand that two-way communication saves time and resources downstream.

    Our feedback loops do more than solve immediate technical questions. This customer experience helps drive investments into analytical equipment upgrades and motivates us to refine synthetic steps to lower residual impurities batch by batch. By tackling complex peptide assembly problems together, we share the lessons learned among our broader user community. This approach keeps us progressing faster than competitors relying on generic production lines or commodity-focused sales channels.

    Custom lot creation for large pharmaceutical or investigative projects highlights the trust practitioners place in repeatable supply chains. Scale-up efforts for kilograms of Boc-D-Bpa-OH translate to new purification challenges, but with direct control over every step, our chemists can troubleshoot each deviation and replicate a successful batch as often as demand requires. For those developing future therapeutics, this reliability lets them plan advanced studies with confidence.

    Peptide Synthesis Trends and Boc-D-Bpa-OH’s Future Role

    As peptide therapeutics mature, the market pushes for increased amino acid diversity and more robust peptide constructs. Our track record with Boc-D-Bpa-OH stems from decades of conversations with medicinal chemists, structural biologists, and process engineers. Our investment in flexible manufacturing, enhanced analytical controls, and end-user engagement mirror where peptide technology is heading: ever more structurally complex, site-specifically labeled, or crosslinker-modified peptides.

    Photoreactive amino acids like D-Bpa enable chemoproteomics, reversible crosslinking mapping, and labeling of large protein assemblies in situ. Our in-plant chemists continually monitor the latest crosslinking protocols, peptide backbone modifications, and orthogonal deprotection methods. Adapting Boc-D-Bpa-OH production means more than ramping up capacity; it also means boosting technical support and improving impurity control as users develop more ambitious peptide syntheses.

    As more organizations integrate automated peptide synthesizers, manufacturers like us play a key role in tuning building blocks for machine compatibility. We optimize flow, solubility, and powder handling to match automation trends. Direct feedback from downstream production lines drives small, continual improvements that help keep users ahead of technical challenges, from research scale to pilot plant programs. This benefit extends past typical catalog offerings, where standard spec sheets neglect rung-by-rung process troubleshooting.

    Practical Solutions for Synthesis Challenges

    Practical issues happen even with a well-tested product like Boc-D-Bpa-OH. In instances where peptide chains stall on the solid phase or unusual byproducts confound isolation, our team steps in with troubleshooting guideline documents—from handling dry powder to swelling bead selection and activation protocol. For photolabeling applications, we collaborate closely with partners on UV irradiation setup, peptide design, and downstream detection, often referencing our own experiments as an internal reference.

    Analysis bottlenecks sometimes threaten program timelines, especially for critical, time-sensitive pharmaceutical projects. To mitigate this, we have expanded our analytical release profile, providing HPLC chromatograms, LC-MS spectra, and impurity tracking for every lot. Many customers report reduced troubleshooting, accelerated method validation, and easier documentation thanks to these datasets. Our technical service group also helps interpret these results, especially when analyzing process deviations or cross-reactivity with coupling reagents.

    We recognize long procurement cycles create workflow gaps, so our logistics team controls safety stock, and our purchasing department maintains back-order protection not just for ourselves but for the accounts relying on seamless peptide production. These investments, born from years of experience, represent ongoing solutions to persistent real-world challenges—not just marketing promises.

    Commitment to Quality and User Trust

    No protected amino acid can claim to solve all synthesis challenges. Boc-D-Bpa-OH solves a specific need: integrating a photoactivatable crosslinker in robust, peptide-based workflows. Our in-house R&D and manufacturing teams routinely test new reaction sequences, examine alternate protection and deprotection workflows, and gather direct user feedback to fix issues at the bench—not just through email or catalogs. Our chemists keep notebooks full of real-world cases, ensuring each process tweak results in a measurable benefit for users.

    Investing in process stability, impurity reduction, and technical literacy sets us apart. Industry experience has taught us that end users value genuine, reliable supply partnerships. Long-term collaboration with leading research and industrial partners has honed our ability to catch quality deviations and technical risks before they reach the end-user’s bench. Integrity matters more than any marketing claim, and our batch traceability, transparency, and robust process documentation reinforce user trust.

    Every year, new researchers and projects bring fresh requirements. Our product, Boc-D-Bpa-OH, carries our reputation inside each batch—defined by the data, validated by experience on the production floor, and sustained by the teams using it in new peptide and protein development efforts. This continual feedback loop drives us to raise standards, push for more regular analytics, and share practical solutions—not just sell a chemical, but build a trusted source for mission-critical synthesis ingredients.