Acetophenone
Structural Formula Vector Image
Title: Acetophenone
CAS Registry Number: 98-86-2
CAS Name: 1-Phenylethanone
Additional Names: phenyl methyl ketone; acetylbenzene; hypnone
Molecular Formula: C8H8O
Molecular Weight: 120.15
Percent Composition: C 79.97%, H 6.71%, O 13.32%
Literature References: Made from benzene and acetylchloride in presence of aluminum chloride; catalytically from acetic and benzoic acids. Prepn from benzene and acetic anhydride: Adams, J. Am. Chem. Soc. 46, 1889 (1924); A. I. Vogel, Practical Organic Chemistry (Longmans, London, 3rd ed., 1959) p 730; Gattermann-Wieland, Die Praxis des Organischen Chemikers (de Gruyter, Berlin, 40th ed., 1961) p 297. Toxicity study: H. F. Smyth, C. P. Carpenter, J. Ind. Hyg. Toxicol. 30, 63 (1948).
Properties: Liquid. Forms laminar crystals at low temp. mp 20.5°. d1515 1.033. bp 202°. nD20 1.5339. Flash pt, closed cup: 221°F (105°C). Slightly sol in water; freely in alcohol, chloroform, ether, fatty oils, glycerol. Sol in concd H2SO4 with orange color. LD50 orally in rats: 0.90 g/kg (Smyth, Carpenter).
Melting point: mp 20.5°
Boiling point: bp 202°
Flash point: Flash pt, closed cup: 221°F (105°C)
Index of refraction: nD20 1.5339
Density: d1515 1.033
Toxicity data: LD50 orally in rats: 0.90 g/kg (Smyth, Carpenter)
Use: In perfumery to impart an orange-blossom-like odor; catalyst for the polymerization of olefins; in organic syntheses, esp. as photosensitizer.

Other Monographs:
Merisoprol Hg 197EpirubicinCupric PerchloratePorofor® BSH
Sodium TripolyphosphateTrichothecinAvidinFenofibrate
ε-Aminocaproic AcidPramipexoleOxetoronen-Butylmalonic Acid
TEMEDCamazepamsym-Trinitrobenzeneo-Nitrophenylpropiolic Acid
©2006-2023 DrugFuture->Chemical Index Database