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Detail of > 589-38-8

  • MSDS Download
  • CAS Number:
  • 589-38-8
  • Name:
  • 3-Hexanone

  • Formula:
  • C6H12 O
  • Molecular Structure:
  • Synonyms:
  • 3-Oxohexane;Ethyl propyl ketone
  • Molecular Weight:
  • 100.18
  • EINECS:
  • 209-645-4
  • Density:
  • 0.815
  • Melting Point:
  • -55°C
  • Boiling Point:
  • 125.5 °C at 760 mmHg
  • Flash Point:
  • 23 ºC
  • Solubility:
  • slightly soluble in water; soluble in acetone; soluble in alcohol and ether in all proportions
  • Appearance:
  • colourless liquid
  • Hazard Symbols:
  • Risk Codes:
  • R11;R36/37/38   
  • Safety:
  • Moderately toxic by ingestion, skin contact, and subcutaneous routes. Mildly toxic by inhalation. A skin and eye irritant. Flammable liquid. A very dangerous fire hazard when exposed to heat or flame; can react vigorously with oxidizing materials. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and fumes. See also KETONES.Details
  • Transport Information:
  • UN 1224
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589-38-8 3-HexanoneCompetitive Product

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589-38-8 3-Hexanone

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589-38-8 3-Hexanone

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589-38-8 3-Hexanone

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    Reference

    Investigations on the effect of oxygen and oxygen-ozone mixtures on the linoleic-linolenic acid model system
    Investigations on the effect of oxygen and oxygen-ozone mixtures on the linoleic-linolenic acid model system. 2. Quantitative determination of peroxides as well as qualitative gas chromatographic investigation of volatile substances. Gruber, H.; Salzer, H.; Mueller-Tyl, E.; Washuettl, J. (Inst. Chem. Technol. Org. St., Tech. Univ. Wien, Vienna, Austria). Seifen, Oele, Fette, Wachse, 104(2), 41-2 (German) 1978. CODEN: SOFWAF. ISSN: 0037-0983. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Aq. emulsions of linoleic acid [60-33-3] or of a linoleic acid-linolenic acid mixt. [66322-05-2] contained peroxides and numerous volatile substances, the amts. of all of which were increased by gassing with O and esp. with O-O3. Gassing with O-O3 produced 23 volatile substances from linolenic acid, and 20 from linoleic acid. Gas chromatog. of the 2,4-dinitrophenylhydrazones of some of these volatiles permitted the identification of AcH [75-07-0], propionaldehyde [123-38-6], propionic acid [79-09-4], 1-hexanal [66-25-1], and 3-hexanone [589-38-8].
    .alpha
    .alpha.-Hydroxyoximes derived from tertiary acetylene alcohols. Chemical and pharmacological studies.In this study, 19849-26-4 and 589-38-8 are also used. Taillandier, Georges; Benoit-Guyod, Jean L.; Boucherle, Andre; Broll, Madeleine; Eymard, Pierre (Lab. Toxicol., Univ. Sci. Med., Grenoble, Fr.). Eur. J. Med. Chem. - Chim. Ther., 11(4), 365-8 (French) 1976. CODEN: EJMCA5. DOCUMENT TYPE: Journal CA Section: 23 (Aliphatic Compounds) Section cross-reference(s): 1 HORR1CR2:NOH (I, R = Me, Et, Pr, R1 = Pr, RR1 = (CH2)5, R = R1 = Et, Bu, R2 = Me) were prepd. by addn. of RR1CO with C2H2 in the presence of a naphthalene anion radical complex, oxidizing RR1C(OH)C.tplbond.CH with HgO, and converting RR1C(OH)Ac to their oximes. I (R-R2 = Pr) was obtained from Grignard reaction of PrBr with (COCl)2 and oximation of HOCPr2COPr. I are anticonvulsants with a more favorable anticonvulsant-hypnotic ratio than phenobarbitol, more favorable muscle relaxant properties than than mephenesine and tranquilizing properties. I (R = Et, R1 = Pr, R2 = Me) was hypnotic at 300 mg/kg in mice. .

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