Acetoin
Structural Formula Vector Image
Title: Acetoin
CAS Registry Number: 513-86-0
CAS Name: 3-Hydroxy-2-butanone
Additional Names: 2,3-butanolone; acetyl methyl carbinol; dimethylketol; g-hydroxy-b-oxobutane
Molecular Formula: C4H8O2
Molecular Weight: 88.11
Percent Composition: C 54.53%, H 9.15%, O 36.32%
Line Formula: CH3CH(OH)COCH3
Literature References: A product of fermentation, also in cream ripened for churning. Obtained by the action of sorbose bacterium or Mycoderma aceti on 2,3-butanediol or by the action of fungi, such as Aspergillus, Penicillium, Mycoderma on sugar cane juice: Browne, J. Am. Chem. Soc. 28, 467 (1906). By action of yeast on diacetyl: Nagelschmidt, Biochem. Z. 186, 317 (1927). From diacetyl by partial reduction with Zn and acid: Diels, Stephan, Ber. 40, 4338 (1907). Fermentation process: Vergnaud, US 2529061 (1950 to Usines de Melle).
Properties: Liquid. Pleasant odor. mp 15°. d417 0.9972. bp760 148°. nD17.3 1.4190. Miscible with water, alcohol. Sparingly sol in ether, petr ether. Reduces Fehling's soln forming acetic acid. Forms a solid dimer C8H16O4 on standing or on treatment with granulated zinc. The dimer is easily converted back to the monomer by melting, distilling or dissolving.
Melting point: mp 15°
Boiling point: bp760 148°
Index of refraction: nD17.3 1.4190
Density: d417 0.9972

Other Monographs:
HafniumOxymetholoneTaurineButobendine
LofepramineRifamidePromethiumFlumedroxone Acetate
1-ChlorohexaneHydroxymercurichlorophenolsNifuraldezoneEndiandric Acids
Neridronic AcidChromic NitratePegvisomantNitrobenzoic Acid
©2006-2023 DrugFuture->Chemical Index Database