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CS-W001157 4
Total: USD 88.00

Boc-Gly-Gly-OH

  • CAS No. 31972-52-8

  • Cat. No. CS-W014684
  • Purity≥97%
  • MDL No.MFCD00038558

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

Boc-Gly-Gly-OH|CS-W014684

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General Information

  • CAS No. 31972-52-8
  • Cat. No. CS-W014684
  • Purity ≥97%
  • MDL No. MFCD00038558
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₆N₂O₅
  • Molecular Weight 232.23
  • Synonym(s) None
  • SMILES CC(C)(OC(NCC(NCC(O)=O)=O)=O)C

Description

Boc-Gly-Gly-OH serves as a key dipeptide building block in peptide synthesis, featuring a stable tert-butoxycarbonyl (Boc) protecting group at the N-terminus and a free C-terminal carboxylic acid. This configuration enables straightforward coupling reactions under standard conditions, with the Boc moiety readily removed via mild acidolysis to reveal the active amine for further elongation. The molecule exhibits excellent bench stability and solubility in common organic solvents, facilitating use in both solution-phase and solid-phase workflows.

Application

Boc-Gly-Gly-OH serves as a reliable dipeptide building block for peptide synthesis, offering bench-stable protection of the N-terminus via the Boc group and a free C-terminal carboxylic acid. Its orthogonal functionality enables straightforward coupling reactions in solid-phase and solution-phase workflows, with high purity and consistent reactivity across standard amide bond formation protocols.

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-H317
Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501

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Computational Chemistry Data

  • TPSA   104.73
  • LogP   -0.2881
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   4

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