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alpha-Azido-omega-hydroxy octa(ethylene glycol)

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alpha-Azido-omega-hydroxy octa(ethylene glycol) Basic information

Product Name:
alpha-Azido-omega-hydroxy octa(ethylene glycol)
Synonyms:
  • Azido-PEG (n=7)
  • O-(2-Azidoethyl)heptaethylene glycol
  • 3,6,9,12,15,18,21-heptaoxatricosan-1-ol,23-azide
  • 23-Azido-3,6,9,12,15,18,21-Heptaoxatricosan-1-ol
  • O-(2-Azidoethyl)heptaethylene glycol >=95% (oligomer purity)
  • Azido-PEG8-alcohol
  • Azide-PEG8-Alcohol
  • Azido-PEG7-alcohol
CAS:
352439-36-2
MF:
C16H33N3O8
MW:
395.45
Product Categories:
  • Aliphatic Azides
  • Alkynes and Other Reagents
  • Azides
  • Building Blocks
  • Chemical Biology
  • Chemical Synthesis
  • Heterobifunctional PEG
  • Conjugation Chemistry: Azides
  • Nitrogen Compounds
  • Organic Building Blocks
  • PEG Azides
  • PEGylation
  • peg
Mol File:
352439-36-2.mol
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alpha-Azido-omega-hydroxy octa(ethylene glycol) Chemical Properties

storage temp. 
2-8°C
solubility 
Soluble in Water, DMSO, DCM, DMF
form 
Liquid
color 
Colorless to light yellow
BRN 
8940056
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
HS Code 
2929900090
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alpha-Azido-omega-hydroxy octa(ethylene glycol) Usage And Synthesis

Description

Azide-PEG8-alcohol is a click chemistry reagent with an azide(N3) and a terminal hydroxyl group. The azide group is reactive with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The hydroxyl (OH) group enables further derivatization or replacement with other functional groups.

Uses

O-(2-Azidoethyl)heptaethylene glycol is used to synthesize oligo and poly(ethylene glycol) derivatives that are used as structural units of dendrimers, hydrogels, surface modifiers, self-assembling systems and molecular crosslinkers. This precursor is compatible for acetylene-azide click reactions.

Some of the reported applications include:

  • Synthesis of strain-stiffening hydrogels through self-assembly of oligomers fibres derived from Azido-PEG (n=7).
  • Synthesis of biodegradable tetra-PEG hydrogels for drug delivery system.
  • Synthesis of heterobifunctional oligo(ethylene glycol) linkers for bioconjugation and targeted drug delivery.
  • Preparation of synthetic amphiphiles for programmed pH-dependent dispersions of carbon nanotubes (CNTs).
  • Selective glycoprotein detection through allosteric click-imprinting by using a self-assembled monolayer developed from the above oligomer.
  • Preparation of bioactivated quantum dot micelles containing fluorescent nanocrystals.

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