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Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid

    • Product Name Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid
    • Alias Fmoc-(R)-4-Bromo-Phe-OH
    • Einecs 831-409-8
    • 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

    926790

    Product Name Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid
    Cas Number 134385-68-9
    Molecular Formula C24H20BrNO4
    Molecular Weight 466.33
    Appearance White to off-white powder
    Purity ≥98%
    Solubility DMSO, DMF, Methanol
    Optical Purity (R)-enantiomer
    Protecting Group Fmoc (Fluorenylmethyloxycarbonyl)
    Storage Temperature 2-8°C
    Synonyms N-Fmoc-(R)-4-bromo-homoalanine
    Application Peptide synthesis
    Functional Group Amino acid derivative
    Smiles C1=CC=C2C(=C1)C=CC3=C2C=CC=C3C(=O)OCC(C(N)CC1=CC=C(C=C1)Br)=O

    As an accredited Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White powder, sealed in an amber glass vial, labeled "Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid, 1g," with hazard and handling instructions.
    Shipping Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid is shipped in sealed, chemical-resistant containers to ensure stability and prevent contamination. The package is labeled according to regulatory guidelines and delivered at room temperature unless otherwise specified. Standard shipping is available worldwide, with expedited and temperature-controlled options upon request.
    Storage Store Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid in a tightly sealed container, protected from light and moisture. Keep at 2-8°C (refrigerator) in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances such as strong acids or bases. Make sure to clearly label the container and follow appropriate safety and handling practices.
    Application of Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid

    Applications of Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid in Industrial Manufacturing

    Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid serves as a key chiral intermediate in industrial peptide synthesis and specialized organic chemistry. As the original producer, we apply validated methods to supply this compound for demanding synthesis routes across regulated industrial sectors. Below, we present precise, real-world downstream applications where this intermediate adds direct manufacturing value, with documented compliance, established dosage guidance, process context, and typical finished products.

    1. Pharmaceutical Peptide Active Pharmaceutical Ingredient (API) Synthesis

    This compound offers a critical enantiopure building block for the industrial synthesis of complex peptides, supporting the development of pharmaceutical APIs targeting therapeutic indications that require non-canonical amino acid incorporation. Manufacturing protocols use it in solid-phase peptide synthesis (SPPS) to introduce functionalized β-amino acid motifs, often in late-stage platform manufacturing for oncology and metabolic disorder drugs.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • cGMP (21 CFR Parts 210/211 US FDA)
    • EP/USP/JP monographs addressing peptide APIs
    • ISO 9001:2015 for quality management in intermediate production

    Typical usage ratio

    • Used at 0.25–2.5 mmol per elongation cycle in SPPS, adjusted to match target sequence length and loading on resin

    Downstream process integration

    • Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid enters the automated peptide synthesizer after resin activation, coupled as one of the programmed amino acid additions prior to Fmoc deprotection and elongation cycles

    Final product types

    • Peptide-based Active Pharmaceutical Ingredients (APIs)
    • Anticancer peptide drugs with modified side chains
    • Metabolic disease peptide therapies

    2. Custom Peptide Reagents for Diagnostic Kit Production

    Diagnostic kit manufacturers require highly pure, sequence-defined peptides containing chiral β-amino acids to enhance specificity and accuracy in immunoassays. Our material supports custom peptide synthesis for MRM standards, peptide calibrators, and in vitro diagnostic reagents. Compliance relies on traceable batch production and validated impurity control, as demanded by quality-focused downstream users in clinical and laboratory assay supply.

    Industry compliance standards

    • ISO 13485:2016 (Medical device and IVD quality management system)
    • IVDR (EU 2017/746 for in vitro diagnostic medical devices)
    • ISO 17025 for reference standard manufacturers
    • Certificate of Analysis supporting traceability for research-use-only (RUO) grade reagents

    Typical usage ratio

    • Blended at 0.1–2% of total peptide content in custom reagent batches, depending on target peptide structure and function in end assay

    Downstream process integration

    • Added during automated or manual peptide chain assembly using Fmoc chemistry, then purified by preparative HPLC prior to lyophilization in diagnostic mixing lines

    Final product types

    • Peptide calibrators for mass spectrometry kits
    • Peptide antigens for enzyme immunoassay kits
    • Reference standards for biomedical diagnostics

    3. Chiral Ligand Precursor for Asymmetric Catalysis Manufacturing

    This amino acid analog is a favored chiral precursor in specialty ligand synthesis for asymmetric catalysis processes. It allows catalyst developers to introduce precise stereochemical control elements critical for pharmaceutical and fine chemical production. Manufacturing partners scale up its use within ligand functionalization toolkits, following established catalyst technology protocols and real process validation steps.

    Industry compliance standards

    • ISO 9001:2015 for chemical synthesis and ligand production QA/QC
    • REACH (EC No 1907/2006) registration for downstream users in the EU
    • Food Contact Materials (Regulation EC 1935/2004) if used in food/intermediate sector catalysis
    • Custom MSDS/CoA documentation for non-pharma catalyst manufacture

    Typical usage ratio

    • Added at 1–8 mol% relative to metal catalyst center, depending on stereochemical control requirements and ligand loading protocols in target catalytic process

    Downstream process integration

    • Serves as a starting chiral subunit in ligand synthesis reactors, functionalized through amide coupling or other organic transformations prior to final catalyst assembly

    Final product types

    • Chiral phosphine or diamine ligands for asymmetric hydrogenation
    • Catalytic intermediates for API and agrochemical production
    • Ligand-controlled synthesis kits for industrial R&D

    4. Specialty Chemical for High-Value Fine Chemical Synthesis

    In the fine chemicals sector, advanced β-amino acid derivatives enable the creation of functionalized organic intermediates with defined halogen patterns. Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid delivers site-specific bromination and stereochemistry, making it suitable for downstream brominated building block production in specialty polymer, agrochemical, and advanced material manufacturing flows. Process engineers optimize its use to maximize yield and stereopurity in challenging multi-step organic syntheses.

    Industry compliance standards

    • ISO 9001:2015 for chemical intermediates production QA
    • REACH Annex VII, VIII or IX registration, based on usage volume in the EU
    • Responsible Care chemical management frameworks
    • HSE process safety requirements for halogenated intermediates

    Typical usage ratio

    • Employed at 0.5–5 mol% in organic synthesis, depending on transformation target, with usage optimized through reaction monitoring and downstream purification constraints

    Downstream process integration

    • Introduced as a key reactant for amide coupling, protection-deprotection cycles, or aryl bromination steps in multi-stage laboratory or pilot scale synthesis

    Final product types

    • Brominated fine chemicals for electronic materials
    • Chiral auxiliaries for crop protection agents
    • High-value specialty intermediates for advanced synthesis supply chains
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