Fmoc-Leu-OH-5,5,5-d3

BR

Reagent Code: #76416
fingerprint
CAS Number 538372-74-6

science Other reagents with same CAS 538372-74-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.43 g/mol
Formula C₂₁H₂₀D₃NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a building block. It is employed to introduce deuterium-labeled leucine residues into peptides, which is useful for studies involving nuclear magnetic resonance (NMR) spectroscopy or mass spectrometry. The deuterium labeling allows for enhanced tracking and analysis of peptide behavior, structure, and interactions in various biochemical and pharmaceutical research applications. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group ensures compatibility with standard SPPS protocols, enabling efficient and selective deprotection during synthesis. This compound is valuable in the development of labeled peptides for drug discovery, metabolic studies, and protein engineering.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,140.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Fmoc-Leu-OH-5,5,5-d3
No image available

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a building block. It is employed to introduce deuterium-labeled leucine residues into peptides, which is useful for studies involving nuclear magnetic resonance (NMR) spectroscopy or mass spectrometry. The deuterium labeling allows for enhanced tracking and analysis of peptide behavior, structure, and interactions in various biochemical and pharmaceutical research applications. Its Fmoc (fluorenylmethyloxycarbonyl) protect

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a building block. It is employed to introduce deuterium-labeled leucine residues into peptides, which is useful for studies involving nuclear magnetic resonance (NMR) spectroscopy or mass spectrometry. The deuterium labeling allows for enhanced tracking and analysis of peptide behavior, structure, and interactions in various biochemical and pharmaceutical research applications. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group ensures compatibility with standard SPPS protocols, enabling efficient and selective deprotection during synthesis. This compound is valuable in the development of labeled peptides for drug discovery, metabolic studies, and protein engineering.

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...