Fmoc-D-Glu(OtBu)-OH

98%

  • Product Code: 66181
  Alias:    N-Fremoxycarbonyl-D-glutamic acid gamma-tert-butyl ester
  CAS:    104091-08-9
Molecular Weight: 425.47 g./mol Molecular Formula: C₂₄H₂₇NO₆
EC Number: MDL Number: MFCD00077055
Melting Point: 83-89 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it serves as a building block for constructing peptides. The Fmoc group protects the amino group during the synthesis process, while the tert-butyl ester group protects the carboxylic acid side chain of glutamic acid. This allows for selective deprotection and coupling steps, enabling the precise assembly of peptide chains. It is commonly employed in the production of therapeutic peptides, research peptides, and peptidomimetics, contributing to advancements in drug development and biochemical studies. Its stability and compatibility with various reagents make it a reliable choice for complex peptide synthesis workflows.
Product Specification:
Test Specification
Melting point 90 94?
PURITYHPLC 98 100%
SPECIFIC ROTATION A20DC1 IN DMF 14 18
APPEARANCE WHITE TO LIGHT YELLOW POWDER
INFRARED SPECTROMETRY Conforms to Structure
TLC ANALYSIS ONE SPOT
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $12.58
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5.000 10-20 days $36.18
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-
25.000 10-20 days $165.96
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Fmoc-D-Glu(OtBu)-OH
Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it serves as a building block for constructing peptides. The Fmoc group protects the amino group during the synthesis process, while the tert-butyl ester group protects the carboxylic acid side chain of glutamic acid. This allows for selective deprotection and coupling steps, enabling the precise assembly of peptide chains. It is commonly employed in the production of therapeutic peptides, research peptides, and peptidomimetics, contributing to advancements in drug development and biochemical studies. Its stability and compatibility with various reagents make it a reliable choice for complex peptide synthesis workflows.
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