2.2.2-Cryptand
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| Names | |
|---|---|
|  Systematic IUPAC name
 4,7,13,16,21,24-Hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane[1]  | |
|  Other names
 Cryptating agent 222  | |
| Identifiers | |
|  23978-09-8  | |
| Abbreviations | Crypt-222 | 
| 620282 | |
| ChemSpider |  65637  | 
| EC Number | 245-962-4 | 
| Jmol 3D model | Interactive image | 
| MeSH | Cryptating+agent+222 | 
| PubChem | 72801 | 
| RTECS number | MP4750000 | 
 
  | |
 
  | |
| Properties | |
|  C 18N 2H 36O 6  | |
| Molar mass | 376.4882 g mol−1 | 
| Melting point | 68 to 71 °C (154 to 160 °F; 341 to 344 K) | 
| Hazards | |
| GHS pictograms |  ![]()  | 
| GHS signal word | WARNING | 
| H315, H319, H335 | |
| P261, P305+351+338 | |
|   EU classification (DSD)  | 
  | 
| R-phrases | R36/37/38 | 
| S-phrases | S26, S36 | 
|   Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  | |
|   | |
| Infobox references | |

Structure of a [2.2.2]cryptand encapsulating a potassium cation (purple). At crystalline state, obtained with an X-ray diffraction.[2]
2.2.2-Cryptand is one of the most important members of the cryptand family of chelating agents. In Nomenclature of Inorganic Chemistry (2005), IUPAC recommends the abbreviation "crypt-222".
References
- ↑ "cryptating agent 222 - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information. Descriptors Computed from Structure.
 - ↑ Alberto, R.; Ortner, K.; Wheatley, N.; Schibli, R.; Schubiger, A. P. (2001). "Synthesis and properties of boranocarbonate: a convenient in situ CO source for the aqueous preparation of [99mTc(OH2)3(CO)3]+". J. Am. Chem. Soc. 121 (13): 3135–3136. doi:10.1021/ja003932b.
 
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