Azido-PEG8-alcohol

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Azido-PEG8-alcohol

Azido-PEG8-alcohol | 352439-36-2

Catelog Number R14-0214
Category Azides
Molecular Formula C16H33N3O8
Molecular Weight 395.45
Catalog Number Size Price Quantity
R14-0214 -- $--

Product Introduction

O-(2-Azidoethyl)heptaethylene glycol (CAS# 352439-36-2) is used in the synthesis of heterobifunctionalized oligo(ethylene glycol) linkers for use in drug delivery.

Chemical Information

Synonyms N3-PEG8-OH;Azide-PEG8-alcohol;2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol
Purity >97%
IUPAC Name 2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol
Canonical SMILES C(COCCOCCOCCOCCOCCOCCOCCO)N=[N+]=[N-]
InChI InChI=1S/C16H33N3O8/c17-19-18-1-3-21-5-7-23-9-11-25-13-15-27-16-14-26-12-10-24-8-6-22-4-2-20/h20H,1-16H2
InChI Key BUMODEBRFGPXRM-UHFFFAOYSA-N
Solubility Water, DMSO, DCM, DMF
Appearance Colorless Liquid
LogP -0.14204

Product Specification

Storage Pure form, -20°C, 3 years; 4°C, 2 years; In solvent, -80°C, 6 months; -20°C, 1 month
Application Applicated in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Monodisperse Azide-PEG8-alcohol (N3-PEG8-OH) is a click chemistry reagent with an azide(N3) and a terminal hydroxyl (OH) 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.
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