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Properties of substance:

1-phenylethanone



skc-file

Synonyms:

acetophenone

Group of substances:

organic

Physical appearance:

colorless liquid

Empirical formula (Hill's system for organic substances):

C8H8O

Structural formula as text:

C6H5C(O)CH3

Molar/atomic mass: 120.15

Melting point (°C):

19.62

Boiling point (°C):

202.3

Solubility (g/100 g of solvent):

acetone: soluble [Ref.]
ammonia liquid : soluble (-33°C) [Ref.]
benzene: soluble [Ref.]
chloroform: soluble [Ref.]
diethyl ether: soluble [Ref.]
diethylamine: miscible [Ref.]
ethanol: 106.6 (0.2°C) [Ref.]
ethanol: 852.4 (11°C) [Ref.]
ethanol: miscible (25°C) [Ref.]
glycerol: soluble [Ref.]
hydrogen fluoride : very soluble [Ref.]
n-butylamine: miscible [Ref.]
tributylamine: miscible [Ref.]
water: 0.5371 (25°C) [Ref.]
water: 0.7937 (60°C) [Ref.]

Density:

1.0281 (20°C, g/cm3)
1.01947 (30°C, g/cm3)
1.015 (35°C, g/cm3)
1.0106 (40°C, g/cm3)
1.0063 (45°C, g/cm3)
1.0021 (50°C, g/cm3)
0.9978 (55°C, g/cm3)

Reactions:

  1. Yeild 75-81%. [Ref.1aster]
    C6H5COCH3 + CH3CHBrCOOC2H5 + Zn → C6H5C(CH3)(OZnBr)CH(CH3)COOC2H5
    C6H5C(CH3)(OZnBr)CH(CH3)COOC2H5 + H2SO4 → C6H5C(CH3)(OH)CH(CH3)COOC2H5 + ZnSO4 + HBr
  2. Yeild 60%. [Ref.1]
    C6H5COCH3 + CH2O + HN(CH3)2 * HCl → C6H5COCH2CH2N(CH3)2 + HCl + H2O
  3. [Ref.1]
    C6H5COCH3 + I2 + 2C5H5N → [C6H5COCH2NC5H5]I + C5H5NHI

Refractive index (nD):

1.53718 (20°C)

Vapour pressure (Torr):

10 (79°C)

Dissociation:

pKa (1) = 19 (20°C, water)

Retention indices for gas chromatography:

1041,5 (phase - 100% dimethylsilicone)
1067,4 (phase - dimethylsilicone with 5% phenyl groups)

Permittivity (dielectric constant):

17.39 (25°C)
8.64 (202°C)

Dipole moment (D):

3.02 (20°C)

Viscosity (mPa·s):

1.511 (30°C)
1.3992 (35°C)
1.1922 (45°C)
1.132 (48°C)

Enthalpy (heat) of vaporization ΔvapH (kJ/mol):

38.79

Heat of combustion (kJ/mol):

4137.6

LD50 (mg/kg):

2650 (white rats, oral)
1250 (mice, oral)

Spectral properties of the substance:

Ultraviolet/visible spectrum (maximum in nm, layer thickness 1 cm, in parentheses - extinction) = 242 (126)
Ultraviolet/visible spectrum (maximum in nm, layer thickness 1 cm, in parentheses - extinction) = 279 (105)
Ultraviolet/visible spectrum (maximum in nm, layer thickness 1 cm, in parentheses - extinction) = 318 (6)

References:

  1. CRC Handbook of Chemistry and Physics. - 90ed. - CRC Press, 2010. - pp. 8-87
  2. Gangolli S. The Dictionary of Substances and their Effects. - 2 ed., Vol. 1, A-B. - RSC, 1999. - pp. 38-39
  3. Lewis R.J. Sax's Dangerous Properties of Industrial Materials. - 11ed. - Wiley-interscience, 2004. - pp. 26
  4. Milne G.W.A. Gardner's Commercially Important Chemicals. - Wiley-Interscience, 2005. - pp. 8
  5. Yalkowsky S.H., Yan H. Handbook of aqueous solubility data. - CRC Press, 2003. - pp. 473
  6. Гордон А., Форд Р. Спутник химика. - М.: Мир, 1976. - pp. 77 [Russian]
  7. Рабинович В.А., Хавин З.Я. Краткий химический справочник. - Л.: Химия, 1977. - pp. 127 [Russian]
  8. Свойства органических соединений: Справочник. - Под ред. Потехина А.А. - Л.: Химия, 1984. - pp. 32-33 [Russian]
  9. Справочник по растворимости. - Т.1, Кн.2. - М.-Л.: ИАН СССР, 1962. - pp. 1228 [Russian]

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    © Collected Ruslan Anatolievich Kiper, burewestnik@mail.ru