Basic information Safety Supplier Related

H2N-PEG2-Propyne

Basic information Safety Supplier Related

H2N-PEG2-Propyne Basic information

Product Name:
H2N-PEG2-Propyne
Synonyms:
  • H2N-PEG2-Propyne
  • HC≡C-CH2-PEG2-NH2
  • Propargyl-PEG2-NH2
  • Propyne-PEG2-amine
  • Alkyne-PEG2-NH2
  • 2-[2-(2-Propynyloxy)ethoxy]ethylamine
  • Propargyl-PEG2-amine
  • 2-(2-(prop-2-yn-1-yloxy)ethoxy)ethan-1-amine
CAS:
944561-44-8
MF:
C7H13NO2
MW:
143.18
Product Categories:
  • Heterobifunctional PEG
  • peg
Mol File:
944561-44-8.mol
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H2N-PEG2-Propyne Chemical Properties

Boiling point:
213.8±20.0 °C(Predicted)
Density 
0.992±0.06 g/cm3(Predicted)
refractive index 
1.4590 to 1.4630
Flash point:
88°
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
DMSO:100.0(Max Conc. mg/mL);698.37(Max Conc. mM)
form 
clear liquid
pka
8.72±0.10(Predicted)
color 
Colorless to Almost colorless
Appearance
colorless to yellow liquid
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Safety Information

RIDADR 
UN 2735 8/PG II
HS Code 
2922.19.9690
HazardClass 
8
PackingGroup 
II
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H2N-PEG2-Propyne Usage And Synthesis

Description

Propargyl-PEG2-amine is a crosslinker that is reactive with NHS esters, carbonyls (carboxylic acid, ketone, aldehyde). The propargyl group can participate in copper catalyzed azide-alkyne Click Chemistry reaction to form a stable triazole linkage.

Uses

2-[2-(2-Propynyloxy)ethoxy]ethylamine is used in preparation of RSV F protein inhibitors conjugated to Fc variants and albumins.

Synthesis

1245006-63-6

944561-44-8

The general procedure for the synthesis of 2-(2-(prop-2-yn-1-yloxy)ethoxy)ethylamine from the compound (CAS:1245006-63-6) is as follows: General method: polymer-loaded triphenylphosphine (1.15 eq.) was added to an anhydrous tetrahydrofuran (THF) solution of azide alkynes S3. Subsequently, the reaction mixture was stirred at room temperature for 48 hours. Next, deionized water (1 mL) was added to the flask and the resulting mixture was continued to be stirred at room temperature for 48 hours. Upon completion of the reaction, the mixture was filtered through a bed of diatomaceous earth to collect insoluble solids and washed with ethyl acetate (25 mL). Finally, the combined filtrates were concentrated under reduced pressure to give the target product aminoalkynes 6.

IC 50

Non-cleavable Linker; PEGs

References

[1] Molecules, 2013, vol. 18, # 9, p. 11639 - 11657
[2] Journal of the American Chemical Society, 2010, vol. 132, # 36, p. 12711 - 12716
[3] Drug Design, Development and Therapy, 2018, vol. 12, p. 987 - 995
[4] Journal of Porphyrins and Phthalocyanines, 2013, vol. 17, # 1-2, p. 104 - 117

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