Weight | 155.241 g/mol |
---|---|
Formula | C9H17NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
826-36-8 (826-36-8)
triacetonamine · tempidon 4-methylbenzenesulfonate · 2,2,6,6-tetramethylpiperidone-4-toluene-p-sulfonate
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- Sigma-Aldrich - 826-36-875.80 - 263.50 USD
- Fisher Scientific - Search for 826-36-8
- TCI - 826-36-824.00 - 151.00 USD
- Triacetonamine formation in a bio-oil from fast pyrolysis of sewage sludge using acetone as the absorption solvent. (Bioresource Technology, 2010)
- 2-aminothiophenes from triacetonamine: A convenient way to novel sterically hindered piperidine derivatives (Heteroatom Chemistry, 1998)
- Triacetonamine formation in fungal extracts. (Journal of Agricultural and Food Chemistry, 1975)
- Formation of diacetonamine and triacetonamine in plant extracts (Phytochemistry, 1967)
- Process for preparing triacetonamine (1974)
- Isolation of triacetonamine from Salsola tetrandra (Phytochemistry, 1971)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H317: May cause an allergic skin reaction
Warning Sensitization, Skin - Category 1 - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 - triacetonamine
- tempidon 4-methylbenzenesulfonate
- 2,2,6,6-tetramethylpiperidone-4-toluene-p-sulfonate
- tempidon sulfate
- tempidon hydrochloride
- TMPone
- 2,2,6,6-tetramethyl-4-piperidone
- tempidon
-
SMILESCC1(CC(=O)CC(N1)(C)C)C
-
InChIKeyJWUXJYZVKZKLTJ-UHFFFAOYSA-N
- Pubchem - 826-36-8
- Wikipedia - triacetonamine
Triacetone amine is the heterocycle that arises via the condensation of acetone and ammonia, with phorone being a likely intermediate. 3 CH3C(O)CH3 + NH3 OC(CH2C(CH3)2)2NH + 2 H2O 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, as well as the radical oxidizer 4-Hydroxy-TEMPO.
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Similar Compounds
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