Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Fmoc-D-Bpa-OH

    • Product Name Fmoc-D-Bpa-OH
    • Alias FDBC10
    • Einecs 242-977-1
    • 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

    889719

    Product Name Fmoc-D-Bpa-OH
    Full Name Fmoc-D-4-Benzoylphenylalanine
    Cas Number 162870-98-8
    Molecular Formula C31H23NO4
    Molecular Weight 473.52
    Appearance White to off-white powder
    Purity ≥98%
    Optical Purity D-isomer
    Protecting Group Fmoc (9-fluorenylmethyloxycarbonyl)
    Functional Group Carboxylic acid
    Solubility Soluble in DMF, DMSO, and other polar organic solvents
    Storage Temperature 2-8°C
    Application Peptide synthesis

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

    Packing & Storage
    Packing Fmoc-D-Bpa-OH is supplied in a sealed amber glass vial, containing 1 gram, labeled with product details and safety information.
    Shipping Fmoc-D-Bpa-OH is shipped in secure, sealed containers under ambient conditions. Packaging ensures protection from moisture, light, and physical damage. For safety, it is labeled according to chemical hazard regulations. Expedited or temperature-controlled shipping may be available upon request. Always check local regulations for receiving chemical substances.
    Storage **Fmoc-D-Bpa-OH** should be stored in a tightly sealed container, protected from light and moisture. Keep at 2–8°C (refrigerator temperature) in a dry, well-ventilated area. Avoid exposure to high temperatures and strong oxidizing agents. Always handle the compound using appropriate personal protective equipment and in accordance with standard laboratory safety protocols.
    Application of Fmoc-D-Bpa-OH

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

    Fmoc-D-Bpa-OH is a specialty-protected amino acid widely adopted in complex peptide synthesis across multiple high-standard downstream industries. As a manufacturer focused on application-driven quality, we support both pioneering pharmaceutical research and established industrial peptide segments with controlled processes and supply consistency. The following sections outline established industrial application scenarios, specifying compliance frameworks, actual formulation parameters, integration stages, and the typical manufactured products benefiting from this compound.

    1. Active Pharmaceutical Ingredient (API) Peptide Synthesis

    Global pharmaceutical peptide manufacturers use Fmoc-D-Bpa-OH as a non-natural residue within therapeutic peptides that require enhanced metabolic stability or specific functional group presentation. Our clients apply it in solid-phase peptide synthesis (SPPS) to design next-generation APIs for clinical and preclinical use, ensuring high batch reliability and purity in regulated environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211
    • USP, EP, JP monograph specifications (as relevant to the peptide product)
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • Introduced at 1 residue per specific sequence; overall inclusion in solid-phase load ranges from 0.5%–5% relative to total amino acid equivalents, depending on target peptide design and allowable modifications by structure-activity data.

    Downstream process integration

    • Deployed during SPPS as a protected amino acid building block; after resin attachment, sequences incorporating D-Bpa allow for orthogonal deprotection and site-specific functionalization steps before final cleavage and purification.

    Final product types

    • Peptide-based APIs for metabolic, oncology, and diagnostic applications
    • Modified peptide fragments for advanced lead optimization
    • Clinical trial investigational peptides

    2. Diagnostic Peptide Reagent Manufacturing

    Fmoc-D-Bpa-OH plays a crucial role in custom peptide synthesis for in-vitro diagnostic (IVD) reagents. Its benzoylphenylalanine moiety enables site-directed photocrosslinking and affinity tagging, supporting production of capture/detection peptides for immunoassays, biosensors, and molecular diagnostics. Downstream manufacturers incorporate it to enhance signal specificity and molecular probe stability.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality Management Systems
    • USP/NF standards for peptide reagents where applicable
    • EU In Vitro Diagnostic Regulation (IVDR) 2017/746
    • Relevant national IVD product registrations

    Typical usage ratio

    • Utilized as a single or repeated building block, usually <1 mol% of total sequence; exact loading varies with probe design and crosslinking function sought in the final peptide structure.

    Downstream process integration

    • Integrated during automated or manual synthesis of short peptide sequences on solid phase, often with protected orthogonal groups to allow subsequent functionalization and post-synthetic labeling, before HPLC purification and lyophilization.

    Final product types

    • Labeled peptide capture agents for ELISA or lateral flow tests
    • Photoaffinity probes for proteomics
    • Crosslinked peptide standards for molecular detection kits

    3. Peptide-based Cosmetic Ingredient Manufacturing

    Fmoc-D-Bpa-OH is incorporated into cosmeceutical peptide sequences requiring D-amino acid motifs, often for improved resilience to enzymatic breakdown and to engineer actives targeting specific dermal pathways. Cosmetic ingredient manufacturers employ it in controlled synthesis protocols to achieve batch-to-batch consistency, providing raw peptide actives for formulators of high-performance topical solutions.

    Industry compliance standards

    • ISO 22716:2007 Cosmetic GMP
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • REACH Regulation (EC) No 1907/2006 for new substances notification
    • Japan Standards of Quasi-drug Ingredients for topical peptides

    Typical usage ratio

    • Normally introduced as 1–2 amino acids within peptides of 5–20 residues; presence in peptide mass ranges from 1%–8% w/w depending on sequence modification strategy and intended stability profile.

    Downstream process integration

    • Added during controlled SPPS cycles, followed by orthogonal deprotection, HPLC purification, and mass spectral QC before blending with cosmetic excipients or exporting as lyophilized powder to cosmetic manufacturing integrators.

    Final product types

    • Anti-aging peptide actives
    • Firming peptide complexes for serums and creams
    • Stabilized peptide fractions for dermal repair products

    4. Peptide-based Biomaterials R&D and Industrial Application

    Academic and industrial material science sectors utilize Fmoc-D-Bpa-OH for structure-activity manipulation in biofunctionalized polymers and engineered biomaterials. Its distinct aromatic scaffold and D-configuration offer enhanced mechanical properties and photochemical reactivity, supporting downstream development of Smart PEGylated gels, tissue scaffolds, and hydrogel matrices that require tailored peptide linkers for performance validation and regulatory submissions.

    Industry compliance standards

    • ISO 10993: Biological Evaluation of Medical Devices
    • FDA QSR 21 CFR Part 820 for medical material producers (where applicable)
    • ASTM F748-06 for biomaterial safety
    • Specific grant or institutional QC protocols for R&D purposes

    Typical usage ratio

    • Introduced as selective anchor sites typically in a range of 0.2–2.5% molar content within native or modified peptide-polymer conjugates; degree of modification depends on desired crosslink density and photoreactive performance metrics.

    Downstream process integration

    • Employed during solid-phase or solution-phase assembly of peptide-based segments, either as a terminal modification or as part of multi-residue linker design; post-assembly, the material undergoes chemical grafting, photo-activation, or cross-linking before downstream processing into bulk material formats.

    Final product types

    • Peptide-functionalized hydrogels
    • Tissue engineering scaffolds
    • Photoreactive polymer-peptide conjugates for controlled cell culture substrates
    Free Quote

    Competitive Fmoc-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.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing Fmoc-D-Bpa-OH: Guiding Synthesis With Experience

    The Role of Fmoc-D-Bpa-OH in Modern Peptide Science

    Drawing from years of bench work and production runs, every chemist quickly appreciates the significance of choosing the exact protecting group and amino acid derivative for solid-phase peptide synthesis. Fmoc-D-Bpa-OH — Fmoc-D-4-Benzoylphenylalanine — stands as one of those specialty tools developed for advanced applications, especially where precise photo-reactivity and structural diversity are required. From the very first batch, we've tailored conditions to preserve enantiomeric purity and to support the demanding standards of research scientists looking for reliability down to the last mg.

    The Fmoc group provides base-labile protection for the amino function of D-4-benzoylphenylalanine, backing streamlined cycles during peptide elongation. The integrity of the D-configuration is confirmed at each synthesis lot, as even small amounts of the L-isomer may skew activity and downstream biological results. With each batch, we verify not only the chemical purity but also chiral homogeneity — a step that sets our process apart from less rigorous sources where D/L ratios may drift with repeated production.

    Model and Specifications Guided by Actual Practice

    We produce Fmoc-D-Bpa-OH under the model number D500, which matches internal reference documentation for traceability across supply batches. Typical product purity exceeds 98% by HPLC, and moisture remains tightly controlled to prevent unwanted side reactions during storage or resin coupling. In our daily operation, we've standardized handling in a dry, inert environment; years ago, overlooked exposure in humid climates led to decreased yields — a lesson now built into every jar as it leaves our facility.

    Our offering typically features crystalline powder, pale off-white, with batch-specific NMR and MS spectra available to support reproducibility. Packaging has evolved, too — switched from HDPE jars to amber glass, after we noticed trace impurities creeping in from polymer containers, particularly after long shipping or warm warehouse storage. Those incremental improvements come directly from customer feedback and internal quality audits, reflecting a product that’s actually made, tested, and refined by lab personnel who actively work with it.

    Why Fmoc-D-Bpa-OH Has Become Indispensable

    Fmoc-D-Bpa-OH has found its place among labs exploring cross-linking, protein-protein interaction mapping, and photoaffinity labeling. The Bpa moiety, a benzophenone group para-substituted on phenylalanine, grants unique light-activated reactivity, allowing researchers to “freeze” interactions under UV irradiation. Such applications require high lots consistency; even minute quantities of unreacted starting material or a small drop in photoactivity can result in ambiguous data, something we’ve worked to eliminate through years of process refinement.

    Customers working with Fmoc-D-Bpa-OH often design peptides that serve as tools rather than therapeutic candidates, but the consequences of inconsistent quality echo throughout drug discovery and biotechnological research. During early production runs, we faced requests for isomeric purity that exceeded peptide market norms — a tough ask, but one which now sits at the core of our QC protocol. Amino acid analysis, chiral HPLC, and photoreactivity tests are run as standard, a direct response to real laboratory needs.

    Standing Apart: Fmoc-D-Bpa-OH Versus Alternative Products

    Many researchers encounter a puzzle when deciding between D and L configurations or between Fmoc and Boc protecting groups. The D-configuration within Fmoc-D-Bpa-OH offers resistance to endogenous protease degradation, crucial for studies in biological matrices or when extending peptide half-life is paramount. We have fielded calls from groups who unintentionally incorporated the L-enantiomer, only to discover rapid loss of signal in their functional assays. This feedback keeps our lot-testing procedures rigorous.

    The Fmoc protection allows for gentle, piperidine-based removal, sidestepping acid-based cleavage that risks damaging acid-sensitive sequences. Labs that moved from Boc chemistry to Fmoc noticed better overall yields and smoother workflows, findings echoed in countless syntheses in our own pilot lines. By focusing on Fmoc-D-Bpa-OH rather than generic, racemic Bpa derivatives, we help reduce synthetic ambiguity while supporting strict analytical validation.

    Best Practices Learned From Production and Collaborative Development

    Stability and storage aren’t just marketing slogans here; we’ve watched batches degrade if not packed and shipped under nitrogen. Some facilities relax those standards, assuming short transit times, but our own experience distributing to humid, tropical regions taught us otherwise. We double-seal each vial — a step earned through years of rework caused by micro-leaks and cap imperfections that let in moisture and air. The oils and dust of a typical warehouse, we learned, can disrupt sensitive photoactive compounds, so cleaning protocols and double-wrapped vials are now non-negotiable.

    Application-wise, tight batch records matter. When one client used an outdated lot, the resulting peptide exhibited faint UV absorbance shifts, jeopardizing weeks of structural and interaction mapping studies. Orederly production history—inclusive of spectral data for every lot—has now become a point of pride, ensuring confidence for repeat buyers. We constantly communicate with users, tweaking protocols to match feedback, and adapting process parameters based on what chemists report from the bench.

    Addressing Synthesis Challenges With Fmoc-D-Bpa-OH

    Solid-phase peptide synthesis remains a precise undertaking. Throughout development, activation conditions and coupling efficiency received significant focus. Early protocols relied on pyrophosphate activation, but this caused unreacted material to persist on-resin. We switched to advanced coupling agents, such as HATU and COMU, after running comparative trials in parallel, reducing capped byproducts and boosting final yield. These lessons wouldn’t have come without batch-scale manufacturing that exposed unforeseen bottlenecks.

    Working at scale means seeing rare impurities emerge with every tenfold increase in output. Our process screens out diketopiperazine formation, with analytical measures built in that originated as a response to rare customer-reported anomalies years back. By tightening the water content to below 0.5% and implementing cascade drying post-crystallization, we cut down side reaction risks. Such operational details aren’t theoretical — they are habits shaped by sustained manufacturing and troubleshooting, reflecting what it means to really support complex lab-scale synthesis.

    Collaboration With Researchers: Real-World Problem Solving

    For bioorganic chemistry labs running photo-crosslinking studies, Fmoc-D-Bpa-OH remains a first-choice amino acid for customizing probe peptides. Early projects often reported challenges with coupling efficiency or sporadic dark decomposition during long reactions. We adapted our purification steps, added inline filtration, and adopted denser glass packaging for international customers. These adaptations involve a continuous cycle of learning from those at the research forefront and responding in real time when unforeseen issues arise.

    We work with protein chemists and structural biologists who demand lot-to-lot reliability. A well-known example stemmed from a project mapping membrane protein-ligand interactions, where a single batch with trace lot variation complicated western blot analyses and forced an entire series of repeat syntheses. We overhauled our batch mixing and sampling protocols, now running retention samples alongside every production lot. This kind of transparency and traceability doesn’t appear overnight — it grows out of direct requests and fielded troubleshooting calls, building an environment where scientific progress isn’t hampered by unpredictable raw materials.

    Analytical Rigor Beyond Standard Industry Norms

    Typical amino acid building blocks may get by with minimal analytical validation, but specialty compounds like Fmoc-D-Bpa-OH warrant deeper investigation. Our labs maintain access to multidimensional NMR, high-resolution mass spectrometry, and chiral chromatography, with annual upgrades driven by the need to keep up with increasingly demanding research partners. Purity means nothing if the isomeric profile fluctuates; those nuances prove decisive in complex structural studies.

    Regular customer visits—by both procurement experts and bench chemists—keep us aware of the variables that matter at the point of synthesis. Insights gleaned from these exchanges filter directly into our analytical priorities. If a research team flags a recurring artifact, we run comparative analyses, updating standard testing to include those signals as necessary. Authenticity in chemical manufacturing emerges from a willingness to learn from every failed batch and a readiness to change when a chemist’s results call current practice into question.

    Tightly Integrated Documentation and Supply-Chain Transparency

    Documentation standards have shifted dramatically over recent decades. Years ago, minimal batch data sufficed, but post-publication reproducibility crises and regulatory audits raised expectations. Each unit of Fmoc-D-Bpa-OH now carries integrated batch certificates, spectral overlays, and proof of analytic milestones met prior to release. Should a customer require further proof, rapid-response teams can track and furnish historic QC records, as organizational protocols demand.

    Managing up-to-date documentation involves more work but brings confidence across the supply chain. From procurement officers to regulators, full traceability helps assure that what arrives in a research lab exactly matches what left our doors. Our process changed only after direct feedback from teams who hit bottlenecks chasing down missing or incomplete documentation. We’ve committed to closing those gaps, making open and verifiable chemical provenance an operational foundation, not an afterthought.

    Operational Improvements Driven by Scientific Dialogue

    Manufacturing specialty products like Fmoc-D-Bpa-OH isn’t just about large vessels and throughput calculations; it revolves around ongoing adjustments based on laboratory realities. Early in our production history, feedback about photo-instability led us to dim-light operations—eventually swapping out harsh fluorescents in post-synthesis areas for low-UV LED bulbs. These changes arose after staff noticed marginal product degradation on final QC, noted only after a series of deep-dive stability investigations requested by an international collaborator.

    Logistical learnings carry equal weight. Delays in customs clearance during monsoon season resulted in moisture ingression, and so we began including humidity indicators in every shipment. Reports of static buildup in dry production climates prompted us to review and upgrade our antistatic handling tools. Over years, these tiny course corrections have shaped a workflow that foregrounds stability, clean handling, and consistent quality on arrival, regardless of geographic distance the product must travel.

    Addressing Industry-Wide Issues: Sourcing Confidence and Scientific Trust

    Quality concerns in peptide building blocks often originate from undermanaged supply chains or patched-together distributor channels. As an actual manufacturer, we maintain rigorous oversight from raw feedstock through final packing, keeping no room for shadow sourcing or ambiguous batch origins. Several customers came to us after less-than-straightforward experiences with resellers, unhappy with inconsistent appearance or unexplained performance drops. Their input fuels our dedication to transparent origin and stable production.

    Market volatility remains another ongoing challenge, with periodic spikes in raw material procurement and shipping disruptions. We’ve responded by securing partnerships upstream — not through brokers or intermediaries, but through directly contracted chemical producers who align with our purity and compliance priorities. Direct relationships flatten communication, permitting immediate resolution when process or analysis insights from researchers call for quick process pivots. This layered integration diminishes the guesswork that clouds standard distributor pipelines.

    Environmental Commitment: Reducing Impact While Ensuring Purity

    Lab-based manufacturing experience clarifies how small changes in environmental practices create outsized effects on both quality and sustainability. In the synthesis of Fmoc-D-Bpa-OH, we moved away from chlorinated solvents for certain washing steps and reduced energy load through batch-reactor heat recovery. Operational tweaks cut down emissions while minimizing byproducts that previously required hazardous waste management. Our staff reuses cleaning solvents wherever analysis supports their reuse, saving expense and supporting responsible practice without fearing cross-contamination.

    Waste stream management now follows updated protocols mapped out after internal audits spotted improvement opportunities during scale-up. Renewable energy supplies a growing portion of our electricity footprint, reflecting the broader responsibility that being a manufacturer entails. Scientists demand both high-fidelity chemicals and responsible production; our process now embraces both sides, tracking environmental data by batch for those who care about sustainable science.

    Supporting the Next Generation of Peptide Science

    Fmoc-D-Bpa-OH’s story is still being written in peptide chemistry labs worldwide, and we continue to learn with, and from, our partners. Recent collaborations have helped us refine analytical methods for faster lot-release cycles without sacrificing the thoroughness that advanced photochemical projects demand. By remaining anchored in production reality, we maintain an adaptable, responsive approach to improvements that matter for both science and the people behind it.

    Everything described—from analytical depth to packaging advances—emerged from the granular work of laboratory synthesis and actual feedback from those applying our product at the bench. As peptide application spaces widen and new structural or therapeutic challenges appear, we continue adjusting practices to ensure that researchers move forward with confidence. Fmoc-D-Bpa-OH stands as a testament to those collective efforts, driven by honest feedback, careful production, and an ongoing commitment to scientific advancement.