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CAS No 98-86-2 , 1-phenylethanone

  • Name: 1-phenylethanone
  • Synonyms: 1-phenylethanone; Phenyl methyl ketone; Acetylbenzene; Benzoyl methide; 1-phenyl-; Ethanone; Methyl phenyl ketone; 98-86-2;1-Phenylethanone; Acetophenon;
  • CAS Registry Number:
  • Transport: 200kgs
  • Melting Point: 19.6 ºC
  • Flash Point: 77 ºC
  • Boiling Point: 202 ºC
  • Density: 1.0266
  • Refractive index: 1.5315-1.534
  • Water Solubility: 5.5 G/L (20 ºC)
  • Safety Statements: R22;R36
  • Hazard Symbols: Xn: Harmful;
  • HS Code: 29143900
  • Flash Point: 77 ºC
  • EINECS: 202-708-7
  • Molecular Weight: 120.14852
  • InchiKey: KWOLFJPFCHCOCG-UHFFFAOYSA-N
  • InChI: InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3
  • Risk Statements: S26
  • Molecular Formula: C8H8O
  • Molecular Structure:CAS No:98-86-2 1-phenylethanone

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References of 1-phenylethanone
Title: Acetophenone
CAS Registry Number: 98-86-2
CAS Name: 1-Phenylethanone
Synonyms: 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.