Chemistry:Triacetonamine
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| Names | |
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| Preferred IUPAC name
2,2,6,6-Tetramethylpiperidin-4-one | |
| Other names
Triacetone amine
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| Properties | |
| C9H17NO | |
| Molar mass | 155.241 g·mol−1 |
| Appearance | Colorless low-melting solid |
| Density | 0.882 g/cm3 |
| Melting point | 43 °C (109 °F; 316 K) |
| Boiling point | 205 °C (401 °F; 478 K) |
| Moderate | |
| Solubility in other solvents | Most organic solvents |
| Hazards | |
| Main hazards | flammable |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H290, H302, H314, H315, H317, H319, H335, H412 | |
| P234, P260, P261, P264, P270, P271, P272, P273, P280, P301+312, P301+330+331, P302+352, P303+361+353, P304+340, P305+351+338, P310, P312, P321, P330, P332+313, P333+313, P337+313, P362, P363, P390 | |
| Flash point | 73 °C; 164 °F; 346 K |
| Related compounds | |
Related compounds
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Piperidine |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Triacetonamine is an organic compound with the formula OC(CH2CMe2)2NH (where Me = CH3). It is a colorless or white solid that melts near room temperature. The compound is an intermediate in the preparation of 2,2,6,6-tetramethylpiperidine, a sterically hindered base and precursor to the reagent called TEMPO. Triacetonamine is formed by the poly-aldol condensation of acetone in the presence of ammonia and calcium chloride:[1]
- 3 (CH3)2CO + NH3 → OC(CH2CMe2)2NH + 2 H2O
Reductive amination of triacetonamine gives 4-amino-2,2,6,6-tetramethylpiperidine.
It is primarily used as a stabilizer for plastics, typically via its conversion to number of hindered amine light stabilizers, but also finds use as a chemical feedstock. It is used to prepare the hindered amine 2,2,6,6-tetramethylpiperidine, CH2[CH2C(CH3)2]2NH,[2] as well as the radical oxidizer 4-Hydroxy-TEMPO.[3]
References
- ↑ Nabyl Merbouh; James M. Bobbitt; Christian Brückner (2004). "Preparation of Tetramethylpiperdine-1-oxoammonlum Salts and Their Use as Oxidants in Organic Chemistry. A Review". Organic Preparations and Procedures International 36: 1-31. doi:10.1080/00304940409355369.
- ↑ Sorgi, K. L. "2,2,6,6-Tetramethylpiperidine" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289X.
- ↑ Ciriminna, Rosaria; Pagliaro, Mario (15 January 2010). "Industrial Oxidations with Organocatalyst TEMPO and Its Derivatives". Organic Process Research & Development 14 (1): 245–251. doi:10.1021/op900059x.
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