[2-[2-(Fmoc-amino)ethoxy]ethoxy]acetic acid

97.0%

  • Product Code: 98069
  Alias:    8-[(9H-Fluoren-9-ylmethoxy)carbonylamino]-3,6-dioxa-n-octanoic acid [2-[2-(fluorenylmethoxycarbonylamino)ethoxy]ethoxy]acetic acid Fmocylamino-8-amino-3,6-dioxoctanoic acid
  CAS:    166108-71-0
Molecular Weight: 385.41 g./mol Molecular Formula: C₂₁H₂₃NO₆
EC Number: MDL Number: MFCD01321015
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used in peptide synthesis as a protecting group for amino acids. Its Fmoc (fluorenylmethyloxycarbonyl) group is particularly valuable in solid-phase peptide synthesis, where it helps in the stepwise construction of peptides by protecting the amino group during the coupling reactions. The ethylene glycol linker enhances solubility in organic solvents, facilitating easier handling and purification processes. Additionally, it is employed in the development of peptide-based drugs and biomaterials, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of complex peptides and proteins for research and therapeutic purposes.
Product Specification:
Test Specification
CARBON BY ELEMENTAL ANALYSIS 63 65.5%
OXYGEN BY ELEMENTAL ANALYSIS 23.7-25.5
PURITYHPLC 97 100%
PURITYNEUTRALIZATION TITRATION 96.5-103.5
APPEARANCE WHITE TO OFF-WHITE POWDER CRYSTALS AND/OR CHUNKS
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.500 10-20 days ฿324.00
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-
1.000 10-20 days ฿612.00
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-
[2-[2-(Fmoc-amino)ethoxy]ethoxy]acetic acid
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. Its Fmoc (fluorenylmethyloxycarbonyl) group is particularly valuable in solid-phase peptide synthesis, where it helps in the stepwise construction of peptides by protecting the amino group during the coupling reactions. The ethylene glycol linker enhances solubility in organic solvents, facilitating easier handling and purification processes. Additionally, it is employed in the development of peptide-based drugs and biomaterials, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of complex peptides and proteins for research and therapeutic purposes.
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