Azide-dPEG5-Amine (N₃-dPEG5-NH₂)

Price range: $360.00 through $1,200.00

Azide-dPEG5-Amine (N₃-dPEG5-NH₂) is a heterobifunctional discrete PEG linker containing a terminal azide (N₃) group and a primary amine (NH₂) group separated by a defined PEG5 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-dPEG5-Amine
Abbreviation: N₃-dPEG5-NH₂
Alternative Names: N3-dPEG5-NH2; Azide-dPEG5-Amine; Azido-dPEG5-Amine; Amino-dPEG5-Azide; NH₂-dPEG5-N₃
CAS: 516493-93-9
Physical form: Colorless clear liquid
Molecular weight: 306.36
Solubility: Chloroform, Methanol, Ethanol
Storage: -20°C, dry and protected from light
Purity: Typically ≥95%

N3-dPEG5-NH2

 

Description

General Description

Azide-dPEG5-Amine (N₃-dPEG5-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 PEG5 spacer.

Unlike conventional polydisperse PEG polymers, dPEG linkers have a defined molecular structure and chain length. The PEG5 spacer provides hydrophilicity and spatial separation between the two reactive termini.

The azide functionality 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 can react with NHS esters, activated carboxylic acids, aldehydes, and other amine-reactive compounds. The two different terminal functionalities enable 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 dPEG5 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, 5g