Hexaaza-18-crown-6
| Names | |
|---|---|
| Preferred IUPAC name
1,4,7,10,13,16-Hexaazacyclooctadecane | |
| Other names
hexacyclen | |
| Identifiers | |
3D model (JSmol) |
|
| ChemSpider | |
| ECHA InfoCard | 100.005.494 |
| EC Number |
|
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C12H30N6 | |
| Molar mass | 258.414 g·mol−1 |
| Appearance | white solid |
| Melting point | 201 °C (394 °F; 474 K) |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H315, H319 | |
| P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Hexaaza-18-crown-6 is the macrocyclic ligand with the formula (CH2CH2NH)6. A white solid, this compound has attracted attention as the N6-analogue of 18-crown-6. It functions as a hexadentate ligand in coordination chemistry. It is the parent hexaaza-crown ether.
Its protonated derivatives bind anions via multiple hydrogen bonds.