188
Views
6
CrossRef citations to date
0
Altmetric
Articles

Determination of Abraham model correlations for describing solute transfer into the methyl butyrate mono-solvent at 298 K

, , , , , , , , , , & show all
Pages 792-802 | Received 02 Aug 2019, Accepted 25 Aug 2019, Published online: 28 Aug 2019

References

  • Pena-Pereira F, Tobiszewski M, Eds. The application of green solvents in separation processes. Amsterdam, The Netherlands: Elsevier Science Publishers; 2017. Chapter 1; p. 3–16.
  • Prat D, Wells A, Hayler J, et al. CHEM21 selection guide of classical- and less classical-solvents. Green Chem. 2016;18:288–296.
  • Prat D, Pardigon O, Flemming H-W, et al. Sanofi’s solvent selection guide: a step toward more sustainable processes. Org Proc Res Develop. 2013;17:1517–1525.
  • Liu K, Wang S, Hart E, et al. Development of Abraham model correlations for solute transfer into 2-ethyl-1-hexanol from both water and the gas phase based on measured solubility ratios. Phys Chem Liq. 2019:1–12. Ahead of Print. doi:10.1080/00319104.2018.1564306.
  • Sedov IA, Salikov TM, Wadawadigi A, et al. Abraham model correlations for describing the thermodynamic properties of solute transfer into pentyl acetate based on headspace chromatographic and solubility measurements. J Chem Thermodyn. 2018;124:133–140.
  • Hart E, Klein A, Barrera M, et al. Development of Abraham model correlations for describing the transfer of molecular solutes into propanenitrile and butanenitrile from water and from the gas phase. Phys Chem Liq. 2018;56:821–833.
  • Sedov IA, Magsumov TI, Hart E, et al. Abraham model expressions for describing water-to-diethylene glycol and gas-to-diethylene glycol solute transfer processes at 298.15 K. J Solut Chem. 2017;46:331–351.
  • Hart E, Klein A, Zha O, et al. Determination of Abraham model solute descriptors for monomeric 3,4,5-trimethoxybenzoic acid from experimental solubility data in organic solvents measured at 298.2 K. Phys Chem Liq. 2018;56:381–390.
  • Lee G, Che M, Qian E, et al. Determination of Abraham model solute descriptors for o- acetoacetanisidide based on experimental solubility data in organic mono-solvents. Phys Chem Liq. 2019;57:528–535.
  • Hart E, Lee G, Qian E, et al. Determination of Abraham model solute descriptors for 4- tert-butylbenzoic acid from experimental solubility data in organic mono-solvents. Phys Chem Liq. 2019;57:445–452.
  • Abraham MH, Acree WE Jr, Brumfield M, et al. Deduction of physicochemical properties from solubilities: 2,4- dihydroxybenzophenone, biotin, and caprolactam as examples. J Chem Eng Data. 2015;60:1440–1446.
  • Bowen KR, Stephens TW, Lu H, et al. Experimental and predicted solubilities of 3,4-dimethoxybenzoic acid in select organic solvents of varying polarity and hydrogen-bonding character. Eur Chem Bull. 2013;2:577–583.
  • Chen G, Liang J, Han J, et al. Solubility modeling, solute-solvent interactions, and thermodynamic dissolution properties of p-nitrophenylacetonitrile in sixteen monosolvents at temperatures ranging from 278.15 to 333.15 K. J Chem Eng Data. 2019;64:315–323.
  • Zheng M, Chen J, Chen G, et al. Solubility modeling and solvent effects of allopurinol in 15 neat solvents. J Chem Eng Data. 2018;63:3551–3558.
  • Zheng M, Chen J, Chen G, et al. Solubility modelling and solvent effect for domperidone in twelve green solvents. J Mol Liq. 2018;261:50–56.
  • Anwer MDK, Mohammad M, Fatima F, et al. Solubility, solution thermodynamics and molecular interactions of osimertinib in some pharmaceutically useful solvents. J Mol Liq. 2019;284:53–58.
  • Ahmad A, Raish M, Alkharfy KM, et al. Solubility, solubility parameters and solution thermodynamics of thymoquinone in different mono solvents. J Mol Liq. 2018;272:912–918.
  • Shakeel F, Haq N, Alshehri S, et al. Solubility, thermodynamic properties and solute-solvent molecular interactions of luteolin in various pure solvents. J Mol Liq. 2018;255:43–50.
  • Wu Y, Zhou L, Zhang X, et al. Determination and correlation of the solubility of acetylpyrazine in pure solvents and binary solvent mixtures. J Solut Chem. 2018;47:950–973.
  • Li S, Wang L, Zhu M, et al. Determination and correlation of solubility and thermodynamic properties of trans-cinnamyl alcohol in pure and binary solvents from 253.15 K to 293.15 K. J Chem Eng Data. 2018;63:77–88.
  • Li M, Zhu P, Han D, et al. Temperature and solvent dependent apparent thermodynamic behavior of 2-mercaptomethyl benzimidazole in pure and binary solvents from 283.15 K to 328.15 K. J Mol Liq. 2017;248:501–508.
  • Wu J, Xu R, Yuan X, et al. Equilibrium solubility of dinitolmide in several neat solvents and binary aqueous co-solvent mixtures: experimental determination and thermodynamic analysis. J Chem Thermodyn. 2019;132:373–382.
  • Tong Y, Zhai S, Wang K, et al. Determination and correlation of solubility and solution thermodynamics of saccharin in different pure solvents. J Chem Thermodyn. 2019;133:70–78.
  • Wu Y, Gao J, Yan S, et al. The dissolution behaviour and apparent thermodynamic analysis of diprophylline in pure and mixed solvents. J Chem Thermodyn. 2019;138:297–303.
  • Jagdale SK, Nawale RB. Solubilization and determination of solution thermodynamic properties of itraconazole in different solvents at different temperatures. Drug Dev Ind Pharm. 2019;45:1168–1180.
  • Zou Z, Yu Y, Fang X, et al. Determination and correlation of solubility and solution thermodynamics of musk xylene in different pure solvents. J Chem Thermodyn. 2019;135:205–214.
  • Qian E, Gupta A, Neal R, et al. Development of Abraham model correlations for describing solute transfer into 2-methyl-1-butanol from both water and the gas phase from experimental solubility data for crystalline organic compounds. Phys Chem Liq. 2019:1–13. Ahead of Print. doi:10.1080/00319104.2019.1625050.
  • Fischer R, Jodray M, Qian E, et al. Abraham model correlations for solute transfer into benzyl alcohol from both water and the gas phase. Phys Chem Liq. 2018:1–11. Ahead of Print. doi:10.1080/00319104.2018.1550778.
  • Qian E, Gupta A, Neal R, et al. Abraham model correlations for describing solute transfer into 4- methyl-2-pentanol from both water and the gas phase. J Mol Liq. 2019;278:335–341.
  • Tong X, Woods D, Acree WE Jr, et al. Updated Abraham model correlations for correlating solute transfer into dry butanone and dry cyclohexanone solvents. Phys Chem Liq. 2018;56:571–583.
  • Abraham MH, Acree WE Jr. Descriptors for ferrocene and some substituted ferrocenes. J Mol Liq. 2017;232:325–331.
  • Abraham MH, Acree WE Jr. Gas-solvent and water-solvent partition of trans-stilbene at 298 K. J Mol Liq. 2017;238:58–61.
  • Ulrich N, Endo S, Brown TN, et al. UFZ-LSER database v 3.2.1 [Internet], Leipzig, Germany: Helmholtz Centre for Environmental Research-UFZ; 2017 [cited 2019 Jul 23]. http://www.ufz.de/lserd
  • Grubbs LM, Saifullah M, De La Rosa NE, et al. Mathematical correlations for describing solute transfer into functionalized alkane solvents containing hydroxyl, ether, ester or ketone solvents. Fluid Phase Equilib. 2010;298:48–53.
  • Stovall DM, Givens C, Keown S, et al. Solubility of crystalline nonelectrolyte solutes in organic solvents: mathematical correlation of 4-chloro-3-nitrobenzoic acid and 2-chloro- 5-nitrobenzoic acid solubilities with the Abraham solvation parameter model. Phys Chem Liq. 2005;43:351–360.
  • Charlton AK, Daniels CR, Acree WE Jr, et al. Solubility of crystalline nonelectrolyte solutes in organic solvents: mathematical correlation of acetylsalicylic acid solubilities with the Abraham general solvation model. J Solut Chem. 2003;32:1087–1102.
  • Wilson A, Tian A, Chou V, et al. Experimental and predicted solubilities of 3,4-dichlorobenzoic acid in select organic solvents and in binary aqueous-ethanol mixtures. Phys Chem Liq. 2012;50:324–335.
  • Fritz JS, Lisicki NM. Titration of acids in nonaqueous solvents. Anal Chem. 1951;23:589–591.
  • Hoover KR, Stovall DM, Pustejovsky E, et al. Solubility of crystalline nonelectrolyte solutes in organic solvents - mathematical correlation of 2-methoxybenzoic acid and 4-methoxybenzoic acid solubilities with the Abraham solvation parameter model. Can J Chem. 2004;82:1353–1360.
  • Acree WE Jr, Bowen KR, Horton MY, et al. Computation of Abraham model solute descriptors for 3-methyl-4-nitrobenzoic acid from measured solubility data. Phys Chem Liq. 2017;55:482–491.
  • Daniels CR, Charlton AK, Wold RM, et al. Thermochemical behavior of dissolved carboxylic acid solutes: solubilities of 3-methylbenzoic acid and 4- chlorobenzoic acid in organic solvents. Can J Chem. 2003;81:1492–1501.
  • Flanagan KB, Hoover KR, Garza O, et al. Mathematical correlation of 1-chloroanthraquinone solubilities in organic solvents with the Abraham solvation parameter model. Phys Chem Liq. 2006;44:377–386.
  • Holley K, Acree WE Jr, Abraham MH. Determination of Abraham model solute descriptors for 2-ethylanthraquinone based on measured solubility ratios. Phys Chem Liq. 2011;49:355–365.
  • Coaxum R, Hoover KR, Pustejovsky E, et al. Thermochemical behavior of dissolved carboxylic acid solutes: part 3 - mathematical correlation of 2-methylbenzoic acid solubilities with the Abraham solvation parameter model. Phys Chem Liq. 2004;42:313–322.
  • Charlton AK, Daniels CR, Wold RM, et al. Solubility of crystalline nonelectrolyte solutes in organic solvents: mathematical correlation of 3-nitrobenzoic acid solubilities with the Abraham general solvation model. J Mol Liq. 2005;116:19–28.
  • Hoover KR, Coaxum R, Pustejovsky E, et al. Thermochemical behavior of dissolved carboxylic acid solutes: part 4 - mathematical correlation of 4-nitrobenzoic acid solubilities with the Abraham solvation parameter model. Phys Chem Liq. 2004;42:339–347.
  • Hoover KR, Acree WE Jr, Abraham MH. Mathematical correlation of phenothiazine solubilities in organic solvents with the Abraham solvation parameter model. Phys Chem Liq. 2006;44:367–376.
  • Hernandez CE, Acree WE Jr. Solubility of fluoranthene in organic nonelectrolyte solvents. Comparison of observed versus predicted values based upon mobile order theory. Can J Chem. 1998;76:1312–1316.
  • Acree WE Jr, Abraham MH. Solubility of crystalline nonelectrolyte solutes in organic solvents: mathematical correlation of benzil solubilities with the Abraham general solvation model. J Solution Chem. 2002;31:293–303.
  • Fletcher KA, Pandey S, McHale MER, et al. Solubility of benzil in organic nonelectrolyte solvents. Comparison of observed versus predicted values based upon mobile theory. Phys Chem Liq. 1996;33:181–190.
  • Monarrez CI, Stovall DM, Woo JH, et al. Solubility of xanthene in organic nonelectrolyte solvents: comparison of observed versus predicted values based upon mobile order theory. Phys Chem Liq. 2002;40:703–714.
  • Stephens TW, Loera M, Calderas M, et al. Determination of Abraham model solute descriptors for benzoin based on measured solubility ratios. Phys Chem Liq. 2012;50:254–265.
  • Stovall DM, Acree WE Jr, Abraham MH. Solubility of 9-fluorenone, thianthrene and xanthene in organic solvents. Fluid Phase Equilib. 2005;232:113–121.
  • Fletcher KA, Hernandez CE, Roy LE, et al. Solubility of diphenyl sulfone in organic nonelectrolyte solvents. Comparison of observed versus predicted values based upon the general solvation model. Can J Chem. 1999;77:1214–1217.
  • Blake-Taylor BH, Deleon VH, Acree WE Jr, et al. Mathematical correlation of salicylamide solubilities in organic solvents with the Abraham solvation parameter model. Phys Chem Liq. 2007;45:389–398.
  • Fletcher KA, McHale MER, Coym KS, et al. Solubility of trans-stilbene in organic nonelectrolyte solvents. Comparison of observed versus predicted values based upon mobile order theory. Can J Chem. 1997;75:258–261.
  • De Fina KM, Ezell C, Acree WE Jr. Solubility of ferrocene in organic nonelectrolyte solvents. Comparison of observed versus predicted values based upon mobile order theory. Phys Chem Liq. 2001;39:699–710.
  • Hoover KR, Coaxum R, Pustejovsky E, et al. Thermochemical behavior of dissolved carboxylic acid solutes: part 5-mathematical correlation of 3,5- dinitrobenzoic acid solubilities with the Abraham solvation parameter model. Phys Chem Liq. 2004;42:457–466.
  • Ye S, Saifullah M, Grubbs LM, et al. Determination of the Abraham model solute descriptors for 3,5-dinitro-2-methylbenzoic acid from measured solubility data in organic solvents. Phys Chem Liq. 2011;49:821–829.
  • Wang S, Liu K, Zhang A, et al. Solubility of 4-methyl-3-nitrobenzoic acid in organic mono-solvents: calculation of Abraham model solute descriptors. Phys Chem Liq. 2019. manuscript accepted for publication, doi:10.1080/00319104.2019.166092.
  • Abraham MH, Zissimos AM, Acree WE Jr. Partition of solutes from the gas phase and from water to wet and dry di-n-butyl ether: a linear free energy relationship analysis. Phys Chem Chem Phys. 2001;3:3732–3736.
  • Sprunger LM, Proctor A, Acree WE Jr, et al. Correlation and prediction of partition coefficient between the gas phase and water, and the solvents dry methyl acetate, dry and wet ethyl acetate, and dry and wet butyl acetate. Fluid Phase Equilib. 2008;270:30–44.
  • Abraham MH, Acree WE Jr, Leo AJ, et al. The partition of compounds from water and from air into wet and dry ketones. New J Chem. 2009;33:568–573.
  • Abraham MH, Acree WE Jr, Leo AJ, et al. Partition of compounds from water and from air into the wet and dry monohalobenzenes. New J Chem. 2009;33:1685–1692.
  • Abraham MH, Acree WE Jr, Cometto-Muniz JE. Partition of compounds from water and from air into amides. New J Chem. 2009;33:2034–2043.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.