N-Carbobenzoxy-L-valine Succinimidyl Ester

98%

Reagent Code: #105558
label
Alias Z-Val-OSu
fingerprint
CAS Number 3496-11-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.4 g/mol
Formula C₁₇H₂₀N₂O₆
badge Registry Numbers
MDL Number MFCD00053547
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily used in peptide synthesis as a protective group for amino acids. It facilitates the coupling of valine to other amino acids or peptides by activating the carboxyl group, making it more reactive. The succinimidyl ester group enhances the efficiency of the reaction, ensuring high yields and purity in the final peptide product. It is particularly valuable in solid-phase peptide synthesis, where precise control over the sequence and structure of peptides is crucial. Additionally, it is employed in the development of pharmaceuticals, especially in the creation of peptide-based drugs, due to its ability to maintain the integrity of the amino acid during complex reactions.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White - Almost White Crystal - Powder
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,660.00
inventory 5g
10-20 days ฿680.00
N-Carbobenzoxy-L-valine Succinimidyl Ester
This compound is primarily used in peptide synthesis as a protective group for amino acids. It facilitates the coupling of valine to other amino acids or peptides by activating the carboxyl group, making it more reactive. The succinimidyl ester group enhances the efficiency of the reaction, ensuring high yields and purity in the final peptide product. It is particularly valuable in solid-phase peptide synthesis, where precise control over the sequence and structure of peptides is crucial. Additionally, it is employed in the development of pharmaceuticals, especially in the creation of peptide-based drugs, due to its ability to maintain the integrity of the amino acid during complex reactions.
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...

Cart

No products

Subtotal: ฿0.00
Total ฿0.00 THB