11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE 134179-38-7 C8H18N4O3
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11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE Basic information |
Product Name: | 11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE |
Synonyms: | H2N-PEG(3)-N3;1-Amino-11-azido-3,6,9-trioxaundecane, 2-{2-[2-(2-Azidoethoxy)ethoxy]ethoxy}ethylamine, O-(2-Aminoethyl)-Oμ-(2-azidoethyl)diethylene glycol;1-Amino-11-azido-3,6,9-trioxaundecane;11-Azido-3,6,9-trioxaundecane-1-amine;N3-PEG3-CH2CH2NH2;11-Azido-3,6,9-trioxaundecylamine;2-{2-[2-(2-Azidoethoxy)ethoxy]ethoxy}ethylamine, 1-Amino-11-azido-3,6,9-trioxaundecane;1-Amino-11-azido-3,6,9-trioxaundecane 11-Amino-3,6,9-trioxaundecanyl Azide |
CAS: | 134179-38-7 |
MF: | C8H18N4O3 |
MW: | 218.25 |
EINECS: | |
Product Categories: | Nitric Oxide Reagents;Cross Linking Reagents;Polyethyleneglycol Derivatives;Aliphatics;Amines;Phosphorylating and Phosphitylating Agents |
Mol File: | 134179-38-7.mol |
11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE Chemical Properties |
Boiling point | 198-202°C |
density | 1.10 g/mL at 20 °C(lit.) |
refractive index |
n |
storage temp. | Amber Vial, Refrigerator, Under Inert Atmosphere |
form | Viscous Liquid |
color | Yellow to Pale Brown |
BRN | 4745506 |
InChIKey | FPVCVHVTMPCZTH-UHFFFAOYSA-N |
Safety Information |
Hazard Codes | C,Xi |
Risk Statements | 34 |
Safety Statements | 26-36/37/39-45 |
RIDADR | UN 2735 8/PG 3 |
WGK Germany | 3 |
F | 10-34 |
HazardClass | 8 |
PackingGroup | III |
HS Code | 29299090 |
11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE Usage And Synthesis |
Chemical Properties | Very Pale Yellow Oil |
Uses | A PEG derivative, which contains a free amine that can be conjugated to biological molecules directly by an amide linkage (or via the corresponding isothiocyanate) and an azide that can be reduced to an amine for conjugation to other molecules. PEG derivatives are water soluble. Bifunctional water soluble compounds with flexible dimensions allow for conjugation of small molecules to proteins or molecular probes. 1-amino-11-azido-3,6,9-trioxaundecane can be reacted with small organic molecules for the synthesis of heterobifunctional compounds. It has been used to synthesize a mannose-fluorescein conjugate for the study of cell-surface mannose-specific lectins. |
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