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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: | Azido-PEG3-NH2;11-Azido-3,6,9-trioxaundecylamine 97%;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 | | CAS: | 134179-38-7 | | MF: | C8H18N4O3 | | MW: | 218.26 | | EINECS: | | Product Categories: | Aliphatics;Amines;Nitric Oxide Reagents;Cross Linking Reagents;Polyethyleneglycol Derivatives;Phosphorylating and Phosphitylating Agents;peg | | 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 | n20/D 1.470 | | storage temp. | Amber Vial, Refrigerator, Under Inert Atmosphere | | form | Viscous Liquid | | color | Yellow to Pale Brown | | BRN | 4745506 | | InChIKey | FPVCVHVTMPCZTH-UHFFFAOYSA-N |
| 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 |
| Description | Amino-PEG3-azide is a bifunctional PEG linker containing an amino group and an azide group. The hydrophilic PEG spacer increases solubility in aqueous media. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. | | 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. | | Uses | 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. |
| 11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE Preparation Products And Raw materials |
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