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Acetylacetone

"Acac" redirects here. For other uses, see ACAC (disambiguation).
Acetylacetone
Skeletal structures of both tautomers
Skeletal structures of both tautomers
Ball-and-stick model of the enol tautomer
Ball-and-stick model of the enol tautomer
Ball-and-stick model of the keto tautomer
Ball-and-stick model of the keto tautomer
Space-filling model of the enol tautomer
Space-filling model of the enol tautomer
Space-filling model of the keto tautomer
Space-filling model of the keto tautomer
Names
IUPAC names
(3Z)-4-Hydroxy-3-penten-2-one (enol form)
Pentane-2,4-dione (keto form)
Other names
  • Hacac
  • 2,4-Pentanedione
Identifiers
3D model (JSmol)
741937
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.004.214 Edit this at Wikidata
EC Number
  • 204-634-0
2537
KEGG
RTECS number
  • SA1925000
UNII
UN number 2310
  • InChI=1S/C5H8O2/c1-4(6)3-5(2)7/h3H2,1-2H3 checkY
    Key: YRKCREAYFQTBPV-UHFFFAOYSA-N checkY
  • InChI=1/C5H8O2/c1-4(6)3-5(2)7/h3H2,1-2H3
    Key: YRKCREAYFQTBPV-UHFFFAOYAO
  • O=C(C)CC(=O)C
  • CC(=O)CC(=O)C
  • Enol form: CC(O)=CC(=O)C
Properties
C5H8O2
Molar mass 100.117 g·mol−1
Appearance Colorless liquid
Density 0.975 g/mL[1]
Melting point −23 °C (−9 °F; 250 K)
Boiling point 140 °C (284 °F; 413 K)
16 g/(100 mL)
−54.88·10−6 cm3/mol
Hazards
GHS labelling:
GHS02: FlammableGHS06: ToxicGHS07: Exclamation markGHS08: Health hazard
Danger
H226, H302, H311, H320, H331, H335, H341, H370, H412
P201, P202, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P281, P301+P312, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P307+P311, P308+P313, P311, P312, P321, P322, P330, P337+P313, P361, P363, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
2
0
Flash point 34 °C (93 °F; 307 K)
340 °C (644 °F; 613 K)
Explosive limits 2.4–11.6%
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Acetylacetone is an organic compound with the chemical formula CH3−C(=O)−CH2−C(=O)−CH3. It is classified as a 1,3-diketone. It exists in equilibrium with a tautomer CH3−C(=O)−CH=C(−OH)−CH3. The mixture is a colorless liquid. These tautomers interconvert so rapidly under most conditions that they are treated as a single compound in most applications.[2] Acetylacetone is a building block for the synthesis of many coordination complexes as well as heterocyclic compounds.

  1. ^ "05581: Acetylacetone". Sigma-Aldrich.
  2. ^ Thomas M. Harris (2001). "2,4-Pentanedione". e-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rp030. ISBN 0471936235.

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أسيتيل الأسيتون Arabic Asetilaseton AZ استیل استون AZB Acetylaceton Czech Acetylacetone Danish Acetylaceton German Acetilacetono EO Acetilacetona Spanish استیل استون FA Asetyyliasetoni Finnish

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