Azide-dPEG4-Amine (N₃-dPEG4-NH₂)

Price range: $360.00 through $1,800.00

Azide-dPEG4-Amine (N₃-dPEG4-NH₂) is a heterobifunctional discrete PEG linker containing a terminal azide (N₃) and a primary amine (NH₂) separated by a defined PEG4 spacer. The azide enables CuAAC and copper-free SPAAC click chemistry, while the primary amine provides a reactive site for NHS esters, activated carboxylic acids, aldehydes, and other amine-reactive molecules. It is useful for bioconjugation, protein and peptide modification, drug conjugation, surface functionalization, and linker synthesis.

Product Name: Azide-dPEG4-Amine
Abbreviation: N₃-dPEG4-NH₂
Alternative Names: N3-dPEG4-NH2; Azide-PEG4-Amine; Azido-dPEG4-Amine; Amino-dPEG4-Azide; NH₂-dPEG4-N₃
CAS: 951671-92-4
Physical form: Colorless clear liquid
MF: C10H22N4O4
Molecular weight: 262.31
Azide Reactive Partners: Terminal alkynes, DBCO, BCN and other strained cyclooctynes
Amine Reactive Partners: NHS esters, activated carboxylic acids, aldehydes and other amine-reactive compounds
Click Chemistry: CuAAC and SPAAC
Purity: ≥95%

 

Description

General Description

Azide-dPEG4-Amine (N₃-dPEG4-NH₂) is a heterobifunctional discrete polyethylene glycol linker containing an azide (N₃) at one end and a primary amine (NH₂) at the other, separated by a defined PEG4 spacer.

Unlike conventional polydisperse PEG polymers, dPEG linkers have a defined chain length and molecular structure. The PEG4 spacer provides hydrophilicity and controlled spatial separation between the two reactive groups.

The terminal azide participates in copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) with terminal alkynes and strain-promoted azide-alkyne cycloaddition (SPAAC) with strained cyclooctynes such as DBCO and BCN.

The primary amine provides an independent reactive site for conjugation with NHS esters, activated carboxylic acids, aldehydes, and other amine-reactive compounds. These orthogonal functionalities make N₃-dPEG4-NH₂ useful for sequential conjugation and the construction of well-defined molecular conjugates.

Applications

  • CuAAC click chemistry
  • Copper-free SPAAC click chemistry
  • Bioconjugation
  • Protein and peptide modification
  • Antibody conjugation
  • Drug conjugation
  • Linker synthesis
  • Fluorescent probe conjugation
  • Nanoparticle functionalization
  • Surface modification
  • PROTAC and molecular linker research

Features and Benefits

  • Defined dPEG4 spacer
  • Heterobifunctional azide and amine termini
  • Compatible with CuAAC
  • Compatible with copper-free SPAAC
  • Primary amine for NHS ester coupling
  • Hydrophilic PEG spacer
  • Suitable for orthogonal conjugation
  • Defined molecular structure
  • Useful for multistep bioconjugation

 

Additional information

Package Size

500mg, 1g, 10g