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Boc-D-2,4-Dichlorophenylalanine

    • Product Name Boc-D-2,4-Dichlorophenylalanine
    • Alias Boc-D-Phe(2,4-Cl2)-OH
    • Einecs 867340-3
    • 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

    404122

    Product Name Boc-D-2,4-Dichlorophenylalanine
    Cas Number 163437-44-3
    Molecular Formula C15H17Cl2NO4
    Molecular Weight 362.21 g/mol
    Appearance White to off-white powder
    Purity Typically ≥98%
    Melting Point 120-125°C
    Storage Temperature 2-8°C
    Solubility Soluble in DMSO, methanol, and ethanol
    Protecting Group Boc (tert-butoxycarbonyl)
    Chirality D-configuration
    Synonyms Boc-D-(2,4-dichlorophenyl)alanine
    Chemical Structure Contains a Boc-protected amino acid with 2,4-dichlorophenyl group
    Application Used in peptide synthesis

    As an accredited Boc-D-2,4-Dichlorophenylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Boc-D-2,4-Dichlorophenylalanine is supplied in a 5-gram amber glass bottle with a secure screw cap and tamper-evident seal.
    Shipping Boc-D-2,4-Dichlorophenylalanine is shipped in tightly sealed containers under ambient or recommended temperature conditions. Packaging complies with safety regulations to prevent exposure and contamination. All containers are appropriately labeled and accompanied by relevant documentation, including safety data sheets, ensuring safe transit and handling during storage and transport.
    Storage **Boc-D-2,4-Dichlorophenylalanine** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally refrigerated at 2–8°C. Avoid excessive heat and sources of ignition. Ensure storage is in a well-ventilated area, away from incompatible substances such as strong acids or bases, to maintain chemical stability and purity.
    Application of Boc-D-2,4-Dichlorophenylalanine

    Applications of Boc-D-2,4-Dichlorophenylalanine in Industrial Manufacturing

    Boc-D-2,4-Dichlorophenylalanine serves as a specialized intermediate in demanding downstream manufacturing sectors. As the direct producer, we supply this protected amino acid for advanced synthesis and formulation processes, focusing on pharmaceutical, peptide, chemical biology, and high-value analytical industries. Below, we detail its major real-world industrial applications with a focus on compliance, formulation, downstream chemistry, and final output.

    1. Peptide Drug Synthesis

    Pharmaceutical manufacturers employ this protected chiral amino acid in the stepwise solid-phase and solution-phase synthesis of clinical peptide APIs, especially where non-natural residues improve biological stability or modulate pharmacokinetics. The Boc group offers controlled reactivity during peptide chain elongation, ensuring site-specific incorporation of the dichlorinated moiety. Its use meets regulatory traceability and batch documentation for preclinical and GMP campaign production.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) Analytical Controls
    • USP <797> Sterile Preparation when used for APIs

    Typical usage ratio

    • 0.5–10 mol% based on peptide length and design; ratio adjusted for residue position, hydrophobicity balance, and desired modification frequency.

    Downstream process integration

    • Direct input during automated or manual amino acid coupling cycles using Fmoc/Boc strategies on resin-bound or solution-phase syntheses, followed by selective deprotection steps.

    Final product types

    • Labeled or modified clinical peptide APIs
    • Specialty therapeutic peptide lead compounds
    • Peptide reference standards for QC and batch release

    2. Pharmaceutical Building Block for Small Molecule Synthesis

    Drug discovery teams integrate this compound as a non-natural side chain moiety in the synthesis of investigational new drugs. The chlorine-substituted aromatic ring supports structure-activity relationship (SAR) optimization in small-molecule pipelines targeting kinases and GPCRs. The Boc group provides temporary protection for amidation reactions or stereocontrolled stepwise modifications, before global deprotection at final synthetic stages.

    Industry compliance standards

    • USP <1045> Bulk Pharmaceutical Chemicals
    • OECD GLP for research and preclinical use
    • REACH Registration (for import/export in the EU)
    • Controlled Documentation per internal QA/QC

    Typical usage ratio

    • 1–20 mol% relative to target compound mass; applied according to stoichiometry in stepwise drug analog synthesis campaigns.

    Downstream process integration

    • Engaged in protected amide bond formation, Boc protection/deprotection cycles in multistep batch reactors or automated synthesis platforms for medicinal chemistry workflows.

    Final product types

    • Advanced pharmaceutical intermediates
    • Clinical phase I/II investigational drugs
    • Patent-protected lead molecules for licensing or partnering

    3. High-Purity Custom Peptide Manufacturing for Diagnostic Kits

    Diagnostic kit producers require functionalized peptides with precise non-canonical residues for use in immunoassays, biomarker capture, or labeled probe construction. This material enters synthesis protocols where exactly timed Boc removal supports selective side chain functionalization. High-purity grades meet batch-to-batch consistency requirements for IVD kit registration.

    Industry compliance standards

    • ISO 13485 for medical device and diagnostic manufacturers
    • China FDA (NMPA) IVD registration specifications
    • ISO 9001:2015 for traceability and quality control
    • ANSI/CLSI peptide standardization guidelines

    Typical usage ratio

    • 1–5 mol% of incorporated residues within custom peptide sequence; modified by peptide length and diagnostic probe design.

    Downstream process integration

    • Fed into peptide synthesizer systems, followed by strict HPLC purification and mass spectrometry authentication required for IVD component qualification.

    Final product types

    • Peptide antigens for ELISA plates
    • Biotinylated or fluorescently labeled diagnostic probes
    • Batch-qualified calibration standards

    4. Chemical Biology Probes and Custom Research Tools

    Academic and industrial research groups utilize this raw material in assembling peptide-based probes or affinity tags, often for studying protein-ligand interactions, cellular uptake, or receptor mapping. The dichlorinated aromatic motif, introduced via protected coupling, enables SAR studies in chemical biology, while Boc protection ensures selective downstream sidechain modifications.

    Industry compliance standards

    • Institutional chemical safety protocols
    • Material transfer agreement (where regulated)
    • GMP not required for RUO (research use only) products
    • Responsible care practices per laboratory standards

    Typical usage ratio

    • 0.5–5 mol% based on probe design and labeling density required for research assay sensitivity.

    Downstream process integration

    • Enters manual peptide assembly or automated solid-phase synthesis platforms, with subsequent site-directed labeling, cleavage, and purification for probe validation.

    Final product types

    • Chemical biology research probes
    • Peptide affinity columns for protein isolation
    • Labeled peptides for imaging or tracking studies
    Free Quote

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