Fmoc-Glu(OtBu)-OH

98%

Reagent Code: #105159
label
Alias Fmoc-O-tert-butyl-L-glutamic acid; Fmoc-O-tert-butyl-L-glutamic acid, 5-tert-butyl fluorenylmethoxycarbonyl-L-glutamic acid
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CAS Number 71989-18-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 425.47 g/mol
Formula C₂₄H₂₇NO₆
badge Registry Numbers
EC Number 276-253-8
MDL Number MFCD00037135
thermostat Physical Properties
Melting Point 83-90 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is widely used in solid-phase peptide synthesis (SPPS) as a protected amino acid derivative. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a temporary protecting group for the amino group, while the OtBu (tert-butyl) group protects the carboxyl side chain of glutamic acid. This dual protection allows for selective deprotection during peptide chain assembly, ensuring precise control over the synthesis process. It is particularly valuable in constructing peptides with glutamic acid residues, as it prevents unwanted side reactions and maintains the integrity of the peptide sequence. Additionally, it is employed in the development of peptide-based drugs, biomaterials, and research tools, where high purity and specificity are essential.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 98-100
Water (Karl Fischer) 4
Melting Point 87-95

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿660.00
inventory 25g
10-20 days ฿1,820.00
Fmoc-Glu(OtBu)-OH
This compound is widely used in solid-phase peptide synthesis (SPPS) as a protected amino acid derivative. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a temporary protecting group for the amino group, while the OtBu (tert-butyl) group protects the carboxyl side chain of glutamic acid. This dual protection allows for selective deprotection during peptide chain assembly, ensuring precise control over the synthesis process. It is particularly valuable in constructing peptides with glutamic acid residues, as it prevents unwanted side reactions and maintains the integrity of the peptide sequence. Additionally, it is employed in the development of peptide-based drugs, biomaterials, and research tools, where high purity and specificity are essential.
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