Azide-dPEG10-Amine (N₃-dPEG10-NH₂)

Price range: $150.00 through $1,460.00

Azide-dPEG10-Amine (N₃-dPEG10-NH₂) is a heterobifunctional discrete PEG linker containing a terminal azide (N₃) and a primary amine (NH₂) separated by a defined PEG10 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-dPEG10-Amine
Abbreviation: N₃-dPEG10-NH₂
Alternative Names: N3-dPEG10-NH2; Azide-PEG10-Amine; Azido-dPEG10-Amine; N3-PEG10-NH2; NH₂-dPEG10-N₃
CAS: 912849-73-1
Molecular weight: 526.62
Solubility: Chloroform, Methanol, Ethanol
Storage: -20°C, dry and protected from light
Purity: Typically ≥95%

N3-dPEG10-NH2

 

Description

General Description

Azide-dPEG10-Amine (N₃-dPEG10-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 PEG10 spacer.

Unlike conventional polydisperse PEG polymers, dPEG linkers have a defined chain length and molecular structure. The PEG10 spacer provides hydrophilicity, flexibility, and controlled spatial separation 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 dPEG10 spacer
  • Heterobifunctional azide and amine termini
  • Compatible with CuAAC
  • Compatible with copper-free SPAAC
  • Primary amine for NHS ester coupling
  • Hydrophilic and flexible PEG spacer
  • Suitable for orthogonal conjugation
  • Defined molecular structure
  • Useful for multistep bioconjugation

Additional information

Package Size

100mg, 200mg, 500mg, 1g, 5g