Cat#: CLP-0082
1,11-Diazido-3,6,9-trioxaundecane
Synonyms (s): Azido-PEG3-azido, Bis-PEG3-Azide
Empirical Formula (Hill Notation): C8H16N6O3
Size: 1 g; 5 g
Product Introduction
Molecular Weight | 244.25 |
NACRES | NA.22 |
CAS Number | 101187-39-7 |
MDL Number | MFCD03425545 |
PubChem Substance ID | 329767198 |
Form | Powder |
Reaction Suitability | Reaction type: Click chemistry; Reagent type: Cross-linking reagent |
Smiles String | [N-]=[N+]=NCCOCCOCCOCCN=[N+]=[N-] |
InChI | 1S/C8H16N6O3/c9-13-11-1-3-15-5-7-17-8-6-16-4-2-12-14-10/h1-8H2 |
InChI key | SFMMXKLNFMIUCH-UHFFFAOYSA-N |
Storage Temp. | -20 °C |
Application
Homobifunctional PEG azide click chemistry linker. Azide functional groups will react via a copper catalyzed or strain promoted 1,3-dipolar cycloaddition click reaction with terminal alkynes and cyclooctyne derivatives to yield a stable triazole linkage.
1,11-Diazido-3,6,9-trioxaundecane may be used to synthesize: 1,11-bis[4-(pyren-1-ylmethoxymethyl)-1H-1,2,3-triazole-1-yl]-3,6,9-trioxaundecane, a fluorogenic chemosensor that can selective detect Hg2+ and Ag+ ions in aqueous methanol solution1-amino-11-azido-3,6,9-trioxaundecane, an intermediate to synthesize tetraethylene glycol based bidentate ligand functionalized with dihydrolipoic acid and biotin (DHLA-TEG-biotin)
Safety Information
Signal Word | Warning |
Hazard Classifications | Acute Tox. 4 Oral |
Storage Class Code | 12 - Non Combustible Liquids |
WGK | WGK 3 |
For research use only. Not for clinical use.