Basic information Safety Supplier Related

α,ω-dipropionic acid tetraethylene glycol

Basic information Safety Supplier Related

α,ω-dipropionic acid tetraethylene glycol Basic information

Product Name:
α,ω-dipropionic acid tetraethylene glycol
Synonyms:
  • α,ω-dipropionic acid tetraethylene glycol
  • 4,7,10,13,16-Pentaoxanonadecanedioic Acid
  • alpha, oMega-Dipropionic acid tetraethylene glycol
  • 3-[2-[2-[2-[2-(2-Carboxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propionic Acid
  • Bis-PEG6-acid
  • 3-[2-[2-[2-[2-(2-carboxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid
  • HOOCCH2CH2O-PEG4-CH2CH2COOH
  • COOH-PEG5-COOH
CAS:
439114-13-3
MF:
C14H26O9
MW:
338.35
Product Categories:
  • PEG
  • Aliphatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
439114-13-3.mol
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α,ω-dipropionic acid tetraethylene glycol Chemical Properties

Boiling point:
513.6±50.0 °C(Predicted)
Density 
1.205±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
3.97±0.10(Predicted)
form 
Solid
color 
White to off-white
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Safety Information

HS Code 
2918999090
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α,ω-dipropionic acid tetraethylene glycol Usage And Synthesis

Description

Bis-PEG5-acid is a PEG linker containing two terminal carboxylic acid groups. The hydrophilic PEG spacer increases solubility in aqueous media. The terminal carboxylic acids can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

Uses

A dicarboxylic acid used in the preparation of potent dimeric inhibitors of the PSD-95-NMDA receptor interaction.

Uses

As a dicarboxylic acid, 4,7,10,13,16-Pentaoxanonadecanedioic Acid can be used in the preparation of potent dimeric inhibitors of the PSD-95-NMDA receptor interaction.

Synthesis

439114-12-2

439114-13-3

The general procedure for the synthesis of 4,7,10,13,16-pentaoxa-nineteenthane-1,19-dioic acid from di-tert-butyl 4,7,10,13,16-pentaoxa-nineteenthane-1,19-dioic acid is as follows: tert-butyl 3-{2-[2-[2-(2-{2-[2-(2-tert-butyloxycarbonyl-ethoxy)ethoxy]ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-propionate (6 g, 18.6 mmol) was dissolved in anisole (20 ml) and cooled in an ice bath. Subsequently, trifluoroacetic acid (65 g) was added slowly. The reaction mixture was stirred at room temperature for 3 hours and the volatiles were removed by distillation under reduced pressure. The residue was extracted by partitioning between ethyl acetate (50 ml) and 5% sodium bicarbonate solution. The aqueous layer was acidified with 1N HCl to pH<2, then saturated with NaCl and extracted with ethyl acetate (3 x 50 ml). The organic layers were combined, washed with saturated brine and dried with anhydrous sodium sulfate. Finally, the solvent was removed by distillation under reduced pressure to afford the target product 4,7,10,13,16-pentaoxadecane-1,19-dioic acid as a colorless liquid, which solidified to a white solid after refrigeration (3.8 g, 82% yield).

IC 50

PEGs

References

[1] Patent: US2006/205670, 2006, A1. Location in patent: Page/Page column 103
[2] Patent: US2008/166364, 2008, A1. Location in patent: Page/Page column 104-105

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