Azide-dPEG2-Amine (N₃-dPEG2-NH₂)

Price range: $360.00 through $650.00

Azide-dPEG2-Amine (N₃-dPEG2-NH₂) is a heterobifunctional discrete PEG linker containing a terminal azide (N₃) and a primary amine (NH₂) separated by a defined PEG2 spacer. The azide enables CuAAC and copper-free SPAAC click chemistry, while the primary amine reacts with 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-dPEG2-Amine
Abbreviation: N₃-dPEG2-NH₂
Alternative Names: N3-dPEG2-NH2; Azide-PEG2-Amine; Azido-dPEG2-Amine; Amino-dPEG2-Azide; NH₂-dPEG2-N₃
CAS: 166388-57-4
Physical form: Colorless clear liquid
MF: C6H14N4O2
Molecular weight: 174.2
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-dPEG2-Amine (N₃-dPEG2-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 PEG2 spacer.

Unlike conventional polydisperse PEG polymers, dPEG linkers have a defined chain length and molecular structure. The PEG2 spacer provides a short hydrophilic linker with controlled spacing between the two reactive termini.

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 NHS esters, activated carboxylic acids, aldehydes, and other amine-reactive compounds. The combination of azide and amine functionalities enables orthogonal and sequential conjugation strategies.

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 dPEG2 spacer
  • Heterobifunctional azide and amine termini
  • Compatible with CuAAC
  • Compatible with copper-free SPAAC
  • Primary amine for NHS ester coupling
  • Short hydrophilic PEG spacer
  • Suitable for orthogonal conjugation
  • Defined molecular structure
  • Useful for multistep bioconjugation

Additional information

Package size

500mg, 1g