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2-[2-(2-AZIDOETHOXY)ETHOXY]ETHANOL

2-[2-(2-AZIDOETHOXY)ETHOXY]ETHANOL Structure
  • ₹12502
  • Product name: 2-[2-(2-AZIDOETHOXY)ETHOXY]ETHANOL
  • CAS: 86520-52-7
  • MF: C6H13N3O3
  • MW: 175.18572
  • EINECS:
  • MDL Number:MFCD09753542
  • Synonyms:2-[2-(2-AZIDOETHOXY)ETHOXY]ETHANOL;2-[2-(2-azidoethoxy)ethoxy]ethan-1-ol;1-Azido-8-hydroxy-3,6-dioxaoctane;8-Azido-3,6-dioxaoctanol;2-[2-(2-Azidoethoxy)ethoxy]ethanol solution;8-Azido-3,6-dioxaoctanol solution;Azido-PEG3;Azido-PEG3-alcohol
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 10ML
  • ManufacturerSigma-Aldrich(India)
  • Product number727423
  • Product description2-[2-(2-Azidoethoxy)ethoxy]ethanol solution ~0.5?M in tert-butyl methyl ether
  • Packaging10ML
  • Price₹12502
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 727423 2-[2-(2-Azidoethoxy)ethoxy]ethanol solution ~0.5?M in tert-butyl methyl ether 10ML ₹12502 2022-06-14 Buy

Properties

Flash point :-33℃
storage temp. :2-8°C
solubility :Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form :Oil
color :Colourless to Light Yellow
BRN :4418543
InChIKey :PMNIHDBMMDOUPD-UHFFFAOYSA-N

Safety Information

Symbol(GHS): GHS hazard pictogramsGHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H225 Highly Flammable liquid and vapour Flammable liquids Category 2 Danger GHS hazard pictograms P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
Precautionary statements:
P210 Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

Description

Azido-PEG3-alcohol is a click chemistry PEG linker containing an azide group 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 group enables further derivatization or replacement with other reactive functional groups.

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