| Weight | 100.117 g/mol |
|---|---|
| Formula | C5H8O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
2,4-Pentanedione (123-54-6)
acetylacetone · indium-111-acetylacetone
Score:
#264 in Physics
,
#782 in Chemistry
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- Preparation, Characterization and Antimicrobial Activity Studies on Some Ternary Complexes of Cu(II) with Acetylacetone and Various Salicylic Acids (Synthesis and Reactivity in Inorganic and Metal-organic Chemistry, 1986)
- A Proton Resonance Study of Bis-(acetylacetone)-ethylenediimine and Related Schiff Bases (Journal of the American Chemical Society, 1961)
- Synthesis and properties of some -diketimines derived from acetylacetone, and their metal complexes (Canadian Journal of Chemistry, 1968)
- Structure of acetylacetone by electron diffraction (Journal of the American Chemical Society, 1971)
- Metal isotope effect on metal-ligand vibrations. IV. Metal complexes of acetylacetone (Journal of the American Chemical Society, 1970)
- Structural investigation of the hydrolysis-condensation process of titanium alkoxides Ti(OR)4 (OR = OPr-iso, OEt) modified by acetylacetone. 1. Study of the alkoxide modification (Chemistry of Materials, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - H311: Toxic in contact with skin
Danger Acute toxicity, dermal - Category 3 - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - H412: Harmful to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 3 - acetylacetone
- indium-111-acetylacetone
-
SMILESCC(=O)CC(=O)C
-
InChIKeyYRKCREAYFQTBPV-UHFFFAOYSA-N
- Pubchem - 2,4-Pentanedione
- Wikipedia - acetylacetone
Acetylacetone is an organic compound that exists in two tautomeric forms that interconvert rapidly and are treated as a single compound in most applications. Although the compound is formally named as the diketone form, pentane-2,4-dione, the enol form forms a substantial component of the material and is actually the favored form in many solvents. It is a colourless liquid that is a precursor to acetylacetonate (acac), a common bidentate ligand.
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Safety
Trends
Alternate Names
Estimated Properties
| Boiling Point | 137.02 C | EPA T.E.S.T. |
|---|---|---|
| Density | 0.96 g/cm3 | EPA T.E.S.T. |
| Flash Point | 36.29 C | EPA T.E.S.T. |
| Water Solubility | 139736 mg/L | EPA T.E.S.T. |
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Synthesis
Similar Compounds
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1,3-Cyclohexanedione
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2,5-HEXANEDIONE
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CYCLOPENTANONE
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4-Heptanone
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3-Methyl-2,4-pentanedione
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3-PENTANONE
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2-NONANONE
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2-TRIDECANONE
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2,15-Hexadecanedione
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2-Pentanone, 4-methyl-1,1,1,3,3-d5-
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3-Tetradecanone
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3-Octanone
(541-85-5, 106-68-3)
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5-Chloro-2-pentanone
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8-PENTADECANONE
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6-UNDECANONE
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CYCLOOCTANONE
(502-49-8)
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3-NONANONE
(77110-38-4, 925-78-0)
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CYCLODODECANONE
(830-13-7)
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4-DECANONE
(624-16-8)
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CYCLOPENTADECANONE
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3-DODECANONE
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(109-49-9)
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(3884-71-7)
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2,6-Dimethyl-3,5-heptanedione
(18362-64-6)
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3-Chloropentane-2,4-dione
(1694-29-7)
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3-bromopentane-2,4-dione
(3043-28-5)
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1,4-Cyclohexanedione
(637-88-7)
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butyraldehyde
(123-72-8)
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2 safety hazards
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6-Chloro-2-hexanone
(10226-30-9)
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3-Ethyl-2-pentanone
(6137-03-7)
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Cyclopropyl methyl ketone
(765-43-5)
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4,4-Dimethyl-2-pentanone
(590-50-1)
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2,3-butanedione
(431-03-8)
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Hexanal
(66-25-1)
3 alternate names
3 safety hazards
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2,6-Dimethyl-4-heptanone
(108-83-8, 626-33-5)
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5-Oxohexanenitrile
(10412-98-3)
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4-METHYL-2-HEXANONE
(105-42-0)
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1,2-Cyclopentanedione
(3008-40-0)
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3-METHYL-2-BUTANONE
(563-80-4)
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Decanal
(112-31-2, 112-81-2)
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Heptanal
(111-71-7)
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5-methylcyclohexane-1,3-dione
(4341-24-6)
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5,5-Dimethylhexane-2,4-dione
(7307-04-2)
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OCTADECANAL
(638-66-4)
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(124-19-6)
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(18920-74-6)
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(40624-07-5)
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1118-71-4
(1118-71-4)
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(96-04-8)
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3-Pentylpentane-2,4-dione
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2-Ethylbutanal
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4-Chloro-2-butanone
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(1193-55-1)
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2,4-Pentanedione
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