Basic information Safety Supplier Related

4,7,10,13,16-Pentaoxanonadeca-1,18-diyne

Basic information Safety Supplier Related

4,7,10,13,16-Pentaoxanonadeca-1,18-diyne Basic information

Product Name:
4,7,10,13,16-Pentaoxanonadeca-1,18-diyne
Synonyms:
  • 4,7,10,13,16-Pentaoxanonadeca-1,18-diyne
  • Bis-propargyl-PEG5
  • Alkyne-PEG5-Alkyne
  • PROPARGYL-PEG5-PROPARGYL
  • Propyl ether-PEG3-Propyl ether
  • 1,11-bis(2-propyn-1-oxy)-3,6,9-trioxaundecane
  • Tetraethylene glycol dipropargyl ether
  • Bis-propargyl-PEG4/4,7,10,13,16-Pentaoxanonadeca-1,18-diyne
CAS:
159428-42-9
MF:
C14H22O5
MW:
270.32
Product Categories:
  • peg
Mol File:
159428-42-9.mol
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4,7,10,13,16-Pentaoxanonadeca-1,18-diyne Chemical Properties

Boiling point:
338.7±37.0 °C(Predicted)
Density 
1.043±0.06 g/cm3(Predicted)
storage temp. 
Storage temp. 2-8°C
form 
Liquid
color 
Colorless to light yellow
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Safety Information

HS Code 
2909199090
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4,7,10,13,16-Pentaoxanonadeca-1,18-diyne Usage And Synthesis

Description

Bis-propargyl-PEG5 is a crosslinker containing propargyl groups at both ends. The propargyl groups reacts with azide-bearing compounds or biomolecules via copper catalyzed Click Chemistry to form stable triazole linkages.

Uses

Bis-propargyl-PEG4 is a PEG-based PROTAC linker used in the synthesis of PROTACs. Bis-propargyl-PEG4 is used for the synthesis of demethylvancomycin dimers[1][2]. Bis-propargyl-PEG4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

References

[1] Pearlie BURNETTE, et al. Dimeric immuno-modulatory compounds against cereblon-based mechanisms. WO2020014489A2.
[2] Jiang, et al. Design, synthesis and biological activity of novel demethylvancomycin dimers against vancomycin-resistant enterococcus faecalis. Tetrahedron, 2018: 74(27), 3527–3533.

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