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CS-W001157 4
Total: USD 88.00

Fmoc-PEA

  • CAS No. 329223-23-6

  • Cat. No. CS-0102564
  • Purity≥95%
  • MDL No.MFCD32201129

*For research and further manufacturing use only, not for direct human use.

Fmoc-PEA|CS-0102564

Structure of 329223-23-6

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General Information

  • CAS No. 329223-23-6
  • Cat. No. CS-0102564
  • Purity ≥95%
  • MDL No. MFCD32201129
  • Storage 4°C, sealed storage, away from moisture and light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₇H₁₈NO₆P
  • Molecular Weight 363.30
  • Synonym(s) None
  • SMILES O=C(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)NCCOP(O)(O)=O

Description

Fmoc-PEA delivers a protected amino acid surrogate with enhanced solubility and ease of handling in solid-phase peptide synthesis. The fluorenylmethoxy carbonyl group enables efficient coupling, while the primary amine facilitates rapid chain elongation. This derivative integrates seamlessly into complex peptide architectures under standard conditions.

Application

Fmoc-PEA serves as a versatile building block in solid-phase peptide synthesis, offering a stable, bench-friendly platform for C-terminal amine functionalization. The fluorenylmethoxycarbonyl (Fmoc) group provides orthogonal protection compatible with standard deprotection conditions, while the primary ethylamine linker enables efficient coupling and facile cleavage under mild acidic conditions. Its robust stability and compatibility with diverse reaction environments make it ideal for constructing peptide libraries and complex synthetic scaffolds.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   105.09
  • LogP   2.6344
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   6

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