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13-Azido-2,5,8,11-tetraoxa-tridecane

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13-Azido-2,5,8,11-tetraoxa-tridecane manufacturers

  • azido-mPEG4
  • azido-mPEG4 pictures
  • 2025-06-07
  • CAS:606130-90-9
  • Min. Order: 1g
  • Purity: >98.00%
  • Supply Ability: 1g
13-Azido-2,5,8,11-tetraoxa-tridecane Basic information
Product Name:13-Azido-2,5,8,11-tetraoxa-tridecane
Synonyms:azido-mPEG4;13-Azido-2,5,8,11-tetraoxa-tridecane;MeO-dPEG4)-N3;1-{2-[2-(2-Azidoethoxy)ethoxy]ethoxy}-2-methoxyethane;m-PEG4-Azide;O-(2-Azidoethyl)-Oμ-methyl-triethylene glycol;13-Azido-2,5,8,11-tetraoxatridecane >;m-dPEG??-Azide (Azido-m-dPEG??)
CAS:606130-90-9
MF:C9H19N3O4
MW:233.26486
EINECS:
Product Categories:Monofunctional PEGs;Aliphatic Azides;Alkynes and Other Reagents;Azide;Azides;Building Blocks;Chemical Biology;Chemical Synthesis;Conjugation Chemistry: Azides;Materials Science;Nitrogen Compounds;Organic Building Blocks;PEG Azides;PEGylation;Poly(ethylene glycol) and Poly(ethylene oxide);Polymer Science;Functionalized Oligoethylene Glycol;peg
Mol File:606130-90-9.mol
13-Azido-2,5,8,11-tetraoxa-tridecane Structure
13-Azido-2,5,8,11-tetraoxa-tridecane Chemical Properties
refractive index 1.4500 to 1.4540
storage temp. 2-8°C
form clear liquid
color Colorless to Light yellow to Light orange
α-endmethoxy
Ω-endazide
InChI1S/C9H19N3O4/c1-13-4-5-15-8-9-16-7-6-14-3-2-11-12-10/h2-9H2,1H3
InChIKeyFFOZZVDSANUDAE-UHFFFAOYSA-N
SMILESCOCCOCCOCCOCCN=[N+]=[N-]
CAS DataBase Reference606130-90-9
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HS Code 29299090
Storage Class13 - Non Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
13-Azido-2,5,8,11-tetraoxa-tridecane Usage And Synthesis
Descriptionm-PEG4-azide is a PEG reagent with an azide group. The azide group is reactive with alkyne, BCN, DBCO via Click Chemistry.
Usesm-PEG4-azide (13-Azido-2,5,8,11-tetraoxatridecane) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1]. m-PEG4-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
reaction suitabilityreaction type: click chemistry
reagent type: cross-linking reagent
IC 50PEGs
References[1] Belen Begines, et al. Synthesis of Reduction Sensitive Comb-Like Polyurethanes Using Click Chemistry. Journal of Polymer Science Part A: Polymer Chemistry, 2016, 54(24), 3888-3900.
13-Azido-2,5,8,11-tetraoxa-tridecane Preparation Products And Raw materials
Tag:13-Azido-2,5,8,11-tetraoxa-tridecane(606130-90-9) Related Product Information
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