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| Name | 2,2,6,6-tetramethyl-4-piperidone |
| Category | Pharmaceutical intermediates |
| Basic Information | |
| Synonyms | 4-Piperidinone, 2,2,6,6-tetramethyl-; Tempidon; Triacetonamin; triacetone amine; |
| CAS number | 826-36-8 |
| EINECS | 212-554-2 |
| Formula | C9H17NO |
| Structure |   |
| Molecular Weight | 155.24 |
| Melting Point | 59-61 °C |
| Flashing Point | 73°C |
| Boiling point | 105-105°C/18mm |
| density | 0.9796 g/mL at 25 °C(lit.) |
| COA Information | |
| Apperance | Light Yellow Powder |
| Purity | min. 99% |
| Moisture | max. 1.0% |
| Safety Information | |
| Hazard Codes | C,Xn |
| Risk Statements | 34-22-36/37/38 |
| RTECS | TO0127900 |
| Safety Statements | 45-36/37/39-26-22-36/37 |
| HS Code | 29333990 |
| Description | |
| 2,2,6,6-tetramethyl-4-piperidone 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. | |
| Name | 2,2,6,6-tetramethyl-4-piperidone |
| Category | Pharmaceutical intermediates |
| Basic Information | |
| Synonyms | 4-Piperidinone, 2,2,6,6-tetramethyl-; Tempidon; Triacetonamin; triacetone amine; |
| CAS number | 826-36-8 |
| EINECS | 212-554-2 |
| Formula | C9H17NO |
| Structure | |
| Molecular Weight | 155.24 |
| Melting Point | 59-61 °C |
| Flashing Point | 73°C |
| Boiling point | 105-105°C/18mm |
| density | 0.9796 g/mL at 25 °C(lit.) |
| COA Information | |
| Apperance | Light Yellow Powder |
| Purity | min. 99% |
| Moisture | max. 1.0% |
| Safety Information | |
| Hazard Codes | C,Xn |
| Risk Statements | 34-22-36/37/38 |
| RTECS | TO0127900 |
| Safety Statements | 45-36/37/39-26-22-36/37 |
| HS Code | 29333990 |
| Description | |
| 2,2,6,6-tetramethyl-4-piperidone 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. | |
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