Trt-Dap(Fmoc)-OH

97%

Reagent Code: #243129
fingerprint
CAS Number 1263046-25-8

science Other reagents with same CAS 1263046-25-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 568.672 g/mol
Formula C₃₇H₃₂N₂O₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in solid-phase peptide synthesis as a protected amino acid derivative, enabling selective assembly of complex peptides. The Fmoc group provides temporary protection of the alpha-amine, allowing stepwise chain elongation, while the Trt (trityl) group protects the side chain of diaminopropionic acid, preventing unwanted reactions. Its orthogonal protection scheme is compatible with Fmoc-based strategies, making it ideal for synthesizing peptides with sensitive functional groups or post-translational modifications. Commonly employed in the preparation of peptide-based pharmaceuticals, bioconjugates, and research reagents where precise control over amino acid sequence is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,120.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Trt-Dap(Fmoc)-OH
No image available

Used in solid-phase peptide synthesis as a protected amino acid derivative, enabling selective assembly of complex peptides. The Fmoc group provides temporary protection of the alpha-amine, allowing stepwise chain elongation, while the Trt (trityl) group protects the side chain of diaminopropionic acid, preventing unwanted reactions. Its orthogonal protection scheme is compatible with Fmoc-based strategies, making it ideal for synthesizing peptides with sensitive functional groups or post-translational m

Used in solid-phase peptide synthesis as a protected amino acid derivative, enabling selective assembly of complex peptides. The Fmoc group provides temporary protection of the alpha-amine, allowing stepwise chain elongation, while the Trt (trityl) group protects the side chain of diaminopropionic acid, preventing unwanted reactions. Its orthogonal protection scheme is compatible with Fmoc-based strategies, making it ideal for synthesizing peptides with sensitive functional groups or post-translational modifications. Commonly employed in the preparation of peptide-based pharmaceuticals, bioconjugates, and research reagents where precise control over amino acid sequence is required.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...