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About This Item
Empirical Formula (Hill Notation):
C8H18N4O3
CAS Number:
Molecular Weight:
218.25
UNSPSC Code:
12352125
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4745506
Assay:
≥90% (GC)
Form:
liquid
grade
technical
Quality Level
assay
≥90% (GC)
form
liquid
reaction suitability
reaction type: click chemistry, reagent type: cross-linking reagent
refractive index
n20/D 1.470
density
1.10 g/mL at 20 °C (lit.)
functional group
amine, azide
SMILES string
NCCOCCOCCOCCN=[N+]=[N-]
InChI
1S/C8H18N4O3/c9-1-3-13-5-7-15-8-6-14-4-2-11-12-10/h1-9H2
InChI key
FPVCVHVTMPCZTH-UHFFFAOYSA-N
Application
11-Azido-3,6,9-trioxaundecan-1-amine is an azide with polyethylene glycol-like characteristics that can be used to prepare azide-functionalized polymers via click reaction.
Other Notes
Bifunctional, hydrophilic linker
signalword
Danger
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
flash_point_f
No data available
flash_point_c
No data available
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Synthesis of an O-alkynyl-chitosan and its chemoselective conjugation with a PEG-like amino-azide through click chemistry.
Oliveira JR
Carbohydrate Polymers, 87(1), 240-249 (2012)
Controlled folding of polystyrene single chains: design of asymmetric covalent bridges.
Zamfir M
Polym. Chem., 3(7), 1796-1802 (2012)
C.R. Bertozzi et al.
The Journal of Organic Chemistry, 56, 4326-4326 (1991)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 17758-1ML | 04061838753281 |
| 17758-5ML | 04061838096357 |

