Triacetylmethane
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Names | |
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Other names
3-acetyl-2,4-pentanedione
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
EC Number |
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PubChem CID
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Properties | |
C7H10O3 | |
Molar mass | 142.154 g·mol−1 |
Appearance | colorless liquid |
Density | 1.0591 g/cm3 |
Boiling point | 96–97 °C (205–207 °F; 369–370 K) 15 torr |
Hazards | |
GHS labelling:[1] | |
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Warning | |
H319 | |
P264+P265 | , P280, P305+P351+P338, P337+P317|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Triacetylmethane is the organic compound with the formula HC(C(O)CH3)3. It is a colorless liquid that is soluble in organic solvents and in alkaline water. It readily forms an enolate.[2][3] The enolate forms a variety of metal complexes related to the metal acetylacetonates.[4]
References
- ^ "Triacetylmethane". pubchem.ncbi.nlm.nih.gov.
- ^ Arnett, Edward M.; Maroldo, Stephen G.; Schilling, Steven L.; Harrelson, John A. (1984). "Ion pairing and reactivity of enolate anions. 5. Thermodynamics of ionization of .beta.-di- and tricarbonyl compounds in dimethyl sulfoxide solution and ion pairing of their alkali salts". Journal of the American Chemical Society. 106 (22): 6759–6767. doi:10.1021/ja00334a049.
- ^ Yoshida, Z.; Ogoshi, H.; Tokumitsu, T. (1970). "Intramolecular Hydrogen Bond in Enol Form of 3-Substituted-2,4-Pentanedione". Tetrahedron. 26 (24): 5691–5697. doi:10.1016/0040-4020(70)80005-9.
- ^ Basato, Marino; Caneva, Elisabetta; Tubaro, Cristina; Veronese, Augusto Cesare (2009). "Coordinating Properties of the Anionic Ligand (MeCO)2C(−)C(X)Me (X=O or NH) Toward Transition Metal(II) Centers". Inorganica Chimica Acta. 362 (8): 2551–2555. doi:10.1016/j.ica.2008.11.017.
Categories:
- Articles without InChI source
- Articles without EBI source
- Articles without KEGG source
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- Pages using collapsible list with both background and text-align in titlestyle
- Chembox having GHS data
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- Articles containing unverified chemical infoboxes
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- Triketones
- Chelating agents
- Tridentate ligands
- 3-Hydroxypropenals
- Enols