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Peptide Research Impurity CAS 170643-02-4 Fmoc-D-allo-Thr(tBu)-OH HPLC 99+

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Peptide Research Impurity CAS 170643-02-4 Fmoc-D-allo-Thr(tBu)-OH HPLC 99+

Peptide Research Impurity CAS 170643-02-4 Fmoc-D-allo-Thr(tBu)-OH HPLC 99+
Peptide Research Impurity CAS 170643-02-4 Fmoc-D-allo-Thr(tBu)-OH HPLC 99+

Large Image :  Peptide Research Impurity CAS 170643-02-4 Fmoc-D-allo-Thr(tBu)-OH HPLC 99+ Get Best Price

Product Details:
Place of Origin: CHINA
Brand Name: Enlai Biotech
Certification: ISO 9001 COA HPLC NMR
Payment & Shipping Terms:
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Inside: double PE bag Outside: paper drum
Delivery Time: In Stock
Payment Terms: T/T
Supply Ability: 100 kilograms per month
Detailed Product Description
Product Name: Fmoc-D-allo-Thr(tBu)-OH Molecular Formula: C₂₃H₂₇NO₅
M.W: 397.47 Appearance: White Powder
HPLC: 99% Storage: Room Temp
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Fmoc-D-allo-Thr(tBu)-OH peptide impurity

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CAS 170643-02-4 HPLC standard

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Peptide research impurity with warranty

Peptide Research Impurity CAS 170643-02-4 Fmoc-D-allo-Thr(tBu)-OH HPLC 99+

High-purity Fmoc-D-allo-Thr(tBu)-OH for Impurity Research and peptide development.

Name Fmoc-D-allo-Thr(tBu)-OH
Molecular Formula C₂₃H₂₇NO₅
Molecular Weight 397.47
Appearance White Powder
HPLC Purity 99%+
Synonyms Fmoc-D-allo-Thr(tBu)-OH
Key Applications
  • Fmoc Solid-Phase Peptide Synthesis (SPPS)
    Used as a protected amino acid building block for the stepwise synthesis of peptides using conventional Fmoc-SPPS methodologies.
  • Synthesis of D-allo-Threonine-Containing Peptides
    Provides a controlled method for introducing the D-allo-threonine stereoisomer into peptide sequences where specific stereochemical configuration is required.
  • Stereochemical Modification of Peptides
    Used to replace naturally occurring L-amino acid residues with D-allo-Thr residues to study the effects of stereochemistry on peptide structure and biological properties.
  • Peptide Conformation Studies
    The incorporation of D-allo-Thr can be used in the investigation of peptide backbone conformation, side-chain orientation, and three-dimensional molecular structure.
  • Structure–Activity Relationship (SAR) Research
    Applied in medicinal chemistry and peptide drug discovery to prepare peptide analogues for evaluating the relationship between amino acid configuration and biological activity.
  • Peptide Stability Optimization
    D-amino acid-containing peptide sequences can be investigated for their potential influence on enzymatic stability and resistance to proteolytic degradation.
  • Design of Modified Therapeutic Peptides
    Used as a specialized building block in the development of modified peptide candidates with optimized structural and pharmacological characteristics.
  • Peptide Drug Discovery and Development
    Suitable for early-stage research involving the synthesis and screening of novel peptide sequences, analogues, and related pharmaceutical candidates.
  • Preparation of Complex Peptide Sequences
    Can be incorporated into longer and structurally complex peptide chains where precise protection of the amino and hydroxyl functionalities is necessary.

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