Diacetone alcohol
Diacetone alcohol | |
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IUPAC name 4-Hydroxy-4-methyl-pentan-2-one | |
Other names 2-Pentanone, 4-hydroxy-4-methyl; 4-Hydroxy-2-keto-4-methylpentane; Diacetone alcohol | |
Identifiers | |
CAS number | 123-42-2 |
ChemSpider | 13838151 |
ChEBI | CHEBI:55381 |
RTECS number | SA9100000 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C6H12O2 |
Molar mass | 116.16 g/mol |
Appearance | Colorless liquid |
Odor | odorless |
Density | 0.938 g/cm3 |
Melting point | −47 °C; −53 °F; 226 K |
Boiling point | 166 °C; 331 °F; 439 K |
Solubility in water | moderate |
Solubility | most organic solvents |
Refractive index (nD) | 1.4235 |
Hazards | |
R-phrases | R36 |
S-phrases | S24/25 |
Main hazards | Flammable |
Related compounds | |
Related compounds | Acetone methyl isobutyl ketone |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
Infobox references | |
Diacetone alcohol is a chemical compound with the formula CH3C(O)CH2C(OH)(CH3)2. This liquid is a common synthetic intermediate used for the preparation of other compounds.
It occurs naturally in Sleepy grass (Achnatherum robustum).
Synthesis
First identified by Heintz,[1] its preparation entails the Ba(OH)2-catalyzed condensation of two molecules of acetone[2] It undergoes dehydration to give the α,β-unsaturated ketone, mesityl oxide:[3] Hydrogenation of mesityl oxide gives the industrial solvent, methyl isobutyl ketone ("MIBK").
Uses
It is used in cellulose ester lacquers, particularly of the brushing type, where it produces brilliant gloss and hard film and where its lack of odor is desirable. It is used in lacquer thinners, dopes, wood stains, wood preservatives and printing pastes; in coating compositions for paper and textiles; permanent markers;[4] in making artificial silk and leather; in imitation gold leaf; in celluloid cements; as a preservative for animal tissue; in metal cleaning compounds; in the manufacture of photographic film; and in hydraulic brake fluids, where it is usually mixed with an equal volume of castor oil.
References
- ↑ Heintz, Ann. 169, 114 (1873)
- ↑ Conant, J. B.; Tuttle, N. (1941), "Diacetone Alcohol", Org. Synth.; Coll. Vol. 1: 199
- ↑ Conant, J. B.; Tuttle, N. (1941), "Mesityl Oxide", Org. Synth.; Coll. Vol. 1: 345
- ↑ MSDS: Sharpie Chisel Tip Permanent Marker - "Household products database" US Department of Health and Human Services