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2-Amino-N-(prop-2-yn-1-yl)acetamide hydrochloride

  • CAS No. 1221722-25-3

  • Cat. No. CS-0179644
  • Purity≥97%
  • MDL No.MFCD15209627

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

2-Amino-N-(prop-2-yn-1-yl)acetamide hydrochloride|CS-0179644

Structure of 1221722-25-3

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General Information

  • CAS No. 1221722-25-3
  • Cat. No. CS-0179644
  • Purity ≥97%
  • MDL No. MFCD15209627
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₉ClN₂O
  • Molecular Weight 148.59
  • Synonym(s) 2-aMino-N-(prop-2-ynyl)acetaMide hydrochloride
  • SMILES O=C(NCC#C)CN.[H]Cl

Description

2-Amino-N-(prop-2-yn-1-yl)acetamide hydrochloride features a reactive alkyne handle and a primary amine group, enabling efficient bioconjugation and click chemistry applications. This bench-stable derivative delivers reliable performance in peptide labeling, probe synthesis, and targeted delivery systems under standard conditions.

Application

2-Amino-N-(prop-2-yn-1-yl)acetamide hydrochloride serves as a versatile building block for bioactive molecule synthesis, enabling efficient access to amide-linked scaffolds via standard coupling protocols. The terminal alkyne functionality facilitates CuAAC click chemistry, while the amino and acetamide groups offer orthogonal reactivity for further derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in peptide and heterocyclic synthesis workflows.

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-P405-P501

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Computational Chemistry Data

  • TPSA   55.12
  • LogP   -0.8837
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   2

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