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Fmoc-Bpa-OH

    • Product Name Fmoc-Bpa-OH
    • Alias Fmoc-4-Benzoyl-L-phenylalanine
    • Einecs 242-409-8
    • 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

    404260

    Product Name Fmoc-Bpa-OH
    Full Name Fmoc-4-benzoylphenylalanine
    Cas Number 141524-94-9
    Molecular Formula C31H23NO4
    Molecular Weight 473.52
    Appearance white to off-white powder
    Purity ≥98%
    Protecting Group Fmoc
    Functional Group ketone (benzoyl)
    Usage photo-crosslinking amino acid
    Solubility DMSO, DMF, slightly soluble in methanol
    Storage Temperature 2-8°C
    Synonyms Fmoc-p-benzoyl-L-phenylalanine
    Smiles O=C(O)[C@H](Cc1ccc(cc1)C(=O)c2ccccc2)N(C3=O)C=CC4=CC5=CC=CC=C5C=C34
    Application peptide synthesis

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

    Packing & Storage
    Packing Fmoc-Bpa-OH is supplied in a 1-gram amber glass vial, sealed, with a white screw cap and a printed label.
    Shipping Fmoc-Bpa-OH is shipped as a solid powder in tightly sealed, inert containers to protect from moisture and light. The packaging complies with regulatory standards for safe handling of chemicals. During transit, temperature control may be applied to ensure stability. Accompanying documentation outlines proper storage and safety procedures.
    Storage Fmoc-Bpa-OH should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of moisture. The container must be tightly closed and kept at 2-8°C (refrigerated) to maintain stability. Avoid exposure to incompatible substances such as strong acids and bases. Store under inert atmosphere if possible to prevent degradation.
    Application of Fmoc-Bpa-OH

    Applications of Fmoc-Bpa-OH in Industrial Manufacturing

    As a manufacturer specializing in high-purity Fmoc-Bpa-OH, we supply this protected amino acid derivative to specialized sectors requiring precise photoreactive components for peptide synthesis and structural analysis. Our Fmoc-Bpa-OH has achieved large-scale adoption across several downstream manufacturing contexts, especially in peptide research and biopharmaceutical development. Below are detailed application scenarios highlighting specific industry-driven uses, regulatory compliance, integration points, and resulting product categories.

    1. Photoreactive Crosslinking Peptide Synthesis for Biomedical Research

    Research institutions and biopharmaceutical companies utilize Fmoc-Bpa-OH in solid-phase peptide synthesis (SPPS) to introduce photoreactive benzoylphenylalanine residues into bioactive peptides or protein analogs. These photoreactive sites enable subsequent crosslinking experiments that map protein–protein or protein–ligand interactions, contributing to drug target identification and mechanistic studies. Production requires precise handling and analytical verification to ensure site-specific incorporation and efficient photolabeling upon irradiation.

    Industry compliance standards

    • ISO 13485:2016 Medical Device Quality Management (for research and diagnostics tools)
    • ICH Q7 GMP for Active Pharmaceutical Ingredients (where peptides serve as API or pre-clinical candidates)
    • USP <1047> and Ph. Eur. 5.2.3 for impurity profile monitoring during synthesis
    • Institutional Research Integrity Guidelines (for experimental reproducibility and traceability)

    Typical usage ratio

    • 0.5–5 mol% per total amino acid load, adjusted based on target site density and desired crosslinking resolution

    Downstream process integration

    • Charged into Fmoc-based SPPS cycles at the relevant coupling position using automated or manual synthesizers
    • Monitored for coupling efficiency by in-process HPLC or ninhydrin tests

    Final product types

    • Photoreactive peptides for protein–protein interaction mapping
    • Crosslinked peptide–protein complexes for structural biology studies
    • Biotinylated or fluorescently labeled tracer peptides

    2. Site-Specific Photolabeling in Peptide Drug Lead Optimization

    R&D divisions of pharmaceutical companies implement Fmoc-Bpa-OH to create peptides that act both as drug leads and as molecular probes featuring covalent crosslinking capability upon UV activation. Integration of Bpa allows medicinal chemists to characterize binding orientation and target engagement directly within biological matrices, streamlining lead optimization and supporting regulatory submissions for first-in-class therapeutics.

    Industry compliance standards

    • Good Laboratory Practice (GLP) for Preclinical Safety Testing (OECD, US FDA 21 CFR Part 58)
    • EMA and FDA Guidelines on Peptide Drug Substance Characterization
    • ICH Q2(R1) for Analytical Method Validation
    • USP General Chapter <1121> Peptide Mapping

    Typical usage ratio

    • 1–3 equivalents relative to other amino acids to maximize photolabeling sites while maintaining peptide solubility

    Downstream process integration

    • Inserted at predetermined positions during peptide chain elongation using Fmoc/tBu protection strategy
    • Cleaved and purified peptides subjected to UV crosslinking and LC-MS-based mapping

    Final product types

    • Photolabeled peptide drug candidates
    • Analytical standards for pharmacokinetic studies
    • Reference materials for in vitro/in vivo engagement assays

    3. Solid-State NMR and Mass Spectrometry Probes for Biomolecule Interaction Analysis

    Analytical laboratories and contract research organizations employ Bpa-containing peptides synthesized with Fmoc-Bpa-OH for incorporation into biomolecular probes used in advanced biophysical techniques. These probes, once crosslinked to their targets via photoreactive chemistry, facilitate high-resolution mapping using solid-state NMR and mass spectrometry. This application demands stringent purity and minimal racemization, supporting quantitative structure–activity relationship investigations.

    Industry compliance standards

    • ISO/IEC 17025 for Laboratory Testing Competence
    • US Pharmacopeia <1058> for Analytical Instrument Qualification
    • CFR Title 21 Part 211 for Good Manufacturing Practice in Analytical Sample Preparation (where applicable)
    • Chemical Safety Board Standards for Photoreactive Compound Handling

    Typical usage ratio

    • 1–2 equivalents relative to target label sites, optimized based on probe length and interaction model requirements

    Downstream process integration

    • Smoothed into peptide synthesis cycles; crosslinking performed post-purification under controlled UV exposure
    • Directly subjected to high-field NMR or Orbitrap LC-MS analysis after crosslinked sample preparation

    Final product types

    • Covalently crosslinked peptide–protein complexes for NMR structure elucidation
    • MS-analyzable crosslinking adducts for interactome studies
    • Internal standards for mass spectrometry quantification protocols

    4. Custom Peptide Manufacturing for Diagnostic Assay Kits

    Raw material customers in the diagnostic sector integrate Fmoc-Bpa-OH into custom peptide synthesis workflows, producing specialized photoreactive peptides for kits that detect or capture target biomolecules. By embedding Bpa residues, these peptides offer permanent linkage to binding partners, increasing the stability and reliability of assay readouts used in clinical and research diagnostics.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management in Manufacturing
    • ISO 13485:2016 for Diagnostic Medical Devices
    • CLSI EP05-A3 for Precision Performance of Quantitative Measurement Methods
    • 21 CFR Part 820 for Medical Device Good Manufacturing Practice

    Typical usage ratio

    • 0.5–2 equivalents per peptide sequence, tailored to binding site modeling and assay sensitivity requirements

    Downstream process integration

    • Loaded at selected steps in automated peptide synthesizers; post-synthesis, peptides undergo rigorous HPLC purification and UV-activation protocols to finalize assay-ready conjugates

    Final product types

    • Photoreactive peptide capture agents for ELISA and protein array kits
    • Crosslinked control reagents for lateral flow immunoassays
    • Diagnostic calibration standards featuring covalent peptide–protein complexes
    Free Quote

    Competitive Fmoc-Bpa-OH prices that fit your budget—flexible terms and customized quotes for every order.

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    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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