Thermodynamics Research Center / ThermoML | Journal of Chemical and Engineering Data

Measurement and Correlation of Solubility of Gatifloxacin in 12 Pure Solvents from 273.15 K to 318.15 K

Xu, Renjie, Wang, Jian
J. Chem. Eng. Data 2019, 64, 2, 676-681
ABSTRACT
The solubility of gatifloxacin in twelve pure solvents, including methanol, ethanol, n-propanol, isopropanol, n-butanol, acetone, butanone, acetonitrile, ethyl acetate, 1,4-dioxane, toluene and N,N-dimethylformamide (DMF) was determined by using a isothermal saturation method with temperatures ranging from (273.15 to 318.15) K. The results show that the solubility of gatifloxacin in those twelve pure solvents increases with increasing temperature. At a given temperature range, they gradually decrease in the following order: ethyl acetate greater than DMF greater than butanone greater than acetonitrile greater than n-butanol greater than acetone greater than 1,4-dioxane greater than n-propanol greater than ethanol greater than methanol greater than isopropanol greater than toluene. The (KAT-LSER) model was applied to analyze the effect of the solute-solvent intermolecular interactions on the solubility in those pure solvents. Moreover, the obtained solubility data were correlated with the modified Apelblat equation, h equation. The correlation showed good agreement with experimental
Compounds
# Formula Name
1 C19H22FN3O4 gatifloxacin
2 CH4O methanol
3 C3H8O propan-1-ol
4 C2H6O ethanol
5 C4H10O butan-1-ol
6 C3H8O propan-2-ol
7 C3H6O acetone
8 C4H8O butanone
9 C2H3N acetonitrile
10 C4H8O2 ethyl acetate
11 C4H8O2 1,4-dioxane
12 C7H8 toluene
13 C3H7NO dimethylformamide
Datasets
The table above is generated from the ThermoML associated json file (link above). POMD and RXND refer to PureOrMixture and Reaction Datasets. The compound numbers are included in properties, variables, and phases, if specificied; the numbers refer to the table of compounds on the left.
Type Compound-# Property Variable Constraint Phase Method #Points
  • POMD
  • 1
  • 2
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 4
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 3
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 6
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 5
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 7
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 8
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 9
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 10
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 11
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 7
  • POMD
  • 1
  • 12
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10
  • POMD
  • 1
  • 13
  • Mole fraction - 1 ; Liquid
  • Temperature, K; Liquid
  • Pressure, kPa; Liquid
  • Liquid
  • Crystal - 1
  • Chromatography
  • 10