Chemical Properties of 1,4-Dioxane (CAS 123-91-1)

InChI

InChI=1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2

InChI Key

RYHBNJHYFVUHQT-UHFFFAOYSA-N

Formula

C4H8O2

SMILES

C1COCCO1

Molecular Weight¹

88.11

CAS

123-91-1

Other Names

• 1,4-Diethylene dioxide
• 1,4-Diethyleneoxide
• 1,4-Dioxan
• 1,4-Dioxin, tetrahydro-
• 1,4-dioxacyclohexane
• Di(ethylene oxide)
• Diethylene dioxide
• Diethylene ether
• Diokan
• Dioksan
• Diossano-1,4
• Dioxaan-1,4
• Dioxan
• Dioxan-1,4
• Dioxane-1,4
• Dioxanne
• Dioxyethylene ether
• Glycol ethylene ether
• Glycol ethylene ether 8
• NCI-C03689
• NE 220
• NSC 8728
• Rcra waste number U108
• Tetrahydro-p-dioxin
• UN 1165
• dioxane
• p-Dioxan
• p-Dioxin, tetrahydro-
• p-dioxane
• tetrahydro-1,4-dioxin

• ω : Acentric Factor.
• PAff : Proton affinity (kJ/mol).
• T_ig : Autoignition Temperature (K).
• BasG : Gas basicity (kJ/mol).
• Δ_cH°_liquid : Standard liquid enthalpy of combustion (kJ/mol).
• C_p,gas : Ideal gas heat capacity (J/mol×K).
• C_p,liquid : Liquid phase heat capacity (J/mol×K).
• μ : Dipole Moment (debye).
• η : Dynamic viscosity (Pa×s).
• σ_cond : Electrical conductivity (S/m).
• ε_r : Dielectric Constant (Relative permittivity).
• LFL : Lower Flammability Limit (% in Air).
• UFL : Upper Flammability Limit (% in Air).
• T_flash,cc : Flash Point (Closed Cup Method) (K).
• T_flash,oc : Flash Point (Open Cup Method) (K).
• Δ_fG° : Standard Gibbs free energy of formation (kJ/mol).
• R_g : Radius of Gyration.
• Δ_fH°_gas : Enthalpy of formation at standard conditions (kJ/mol).
• Δ_fH°_liquid : Liquid phase enthalpy of formation at standard conditions (kJ/mol).
• Δ_fusH° : Enthalpy of fusion at standard conditions (kJ/mol).
• Δ_fusH : Enthalpy of fusion at a given temperature (kJ/mol).
• Δ_subH : Enthalpy of sublimation at a given temperature (kJ/mol).
• Δ_vapH° : Enthalpy of vaporization at standard conditions (kJ/mol).
• Δ_vapH : Enthalpy of vaporization at a given temperature (kJ/mol).
• IE : Ionization energy (eV).
• ν : Kinematic viscosity (m²/s).
• log₁₀WS : Log10 of Water solubility in mol/l.
• logP_oct/wat : Octanol/Water partition coefficient.
• McVol : McGowan's characteristic volume (ml/mol).
• NFPA Fire : NFPA Fire Rating.
• NFPA Health : NFPA Health Rating.
• NFPA Safety : NFPA Safety Rating.
• P_c : Critical Pressure (kPa).
• pKa : Log10 of Acid Dissociation Constant.
• P_triple : Triple Point Pressure (kPa).
• P_vap : Vapor pressure (kPa).
• n₀ : Refractive Index.
• ρ_c : Critical density (kg/m³).
• ρ_l : Liquid Density (kg/m³).
• I_np : Non-polar retention indices.
• I_p : Polar retention indices.
• D^*_i : Self diffusion coefficient (m²/s).
• Δ_fusS : Entropy of fusion at a given temperature (J/mol×K).
• S°_gas : Molar entropy at standard conditions (J/mol×K).
• S°_liquid : Liquid phase molar entropy at standard conditions (J/mol×K).
• c_sound,fluid : Speed of sound in fluid (m/s).
• γ : Surface Tension (N/m).
• T_boil : Normal Boiling Point Temperature (K).
• T_c : Critical Temperature (K).
• λ_gas : Gas thermal conductivity (W/m×K).
• λ_liquid : Liquid thermal conductivity (W/m×K).
• T_fus : Normal melting (fusion) point (K).
• T_fus(P) : Melting point (K).
• T_triple : Triple Point Temperature (K).
• U_Qi : UNIQUAC Qi Parameter.
• U_Ri : UNIQUAC Ri Parameter.
• V_c : Critical Volume (m³/kmol).
• Z_c : Critical Compressibility.
• Z_ra : Rackett Parameter.
• ¹: Molecular weight from the IUPAC atomic weights tables.

Contents

1. Physical Properties
2. Temperature Dependent Properties
3. Pressure Dependent Properties
4. Datasets
5. Correlations
6. Similar Compounds
7. Mixtures
8. Sources

Physical Properties

Property	Value	Unit	Source
ω	[0.2793; 0.2880]
ω	0.2880		PSRK revision IV (2005), critical constants and acentric factors of 1000 components Compiled value
ω	0.2793		ChemSep v8.3 pure component data Compiled value
ω	0.2810		KDB
PAff	797.40	kJ/mol	NIST
Tig	[453.15; 453.15]	K
Tig	453.15	K	KDB
Tig	453.15	K	NCMS SOLV-DB
BasG	770.00	kJ/mol	NIST
ΔcH°liquid	[-2363.90; -2186.80]	kJ/mol
ΔcH°liquid	-2362.23 ± 0.99	kJ/mol	NIST
ΔcH°liquid	-2363.90 ± 0.50	kJ/mol	NIST
ΔcH°liquid	-2346.20	kJ/mol	NIST
ΔcH°liquid	-2186.80	kJ/mol	NIST
μ	[0.00; 0.40]	debye
μ	0.00	debye	ChemSep v8.3 pure component data Compiled value
μ	0.40	debye	KDB
η	0.0011960	Pa×s	Excess Molar Volumes and Viscosity Deviations of Binary Liquid Mixtures of 1,3-Dioxolane and 1,4-Dioxane with Butyl Acetate, Butyric Acid, Butylamine, and 2-Butanone at 298.15 K
εr	2.21		NCMS SOLV-DB
LFL	1.97	% in Air	KDB
UFL	22.50	% in Air	KDB
Tflash,cc	[285.15; 296.48]	K
Tflash,cc	296.48	K	KDB
Tflash,cc	285.15	K	NCMS SOLV-DB
Tflash,oc	285.37	K	KDB
ΔfG°	[-181.60; -180.90]	kJ/mol
ΔfG°	-181.60	kJ/mol	ChemSep v8.3 pure component data Compiled value
ΔfG°	-180.90	kJ/mol	KDB
Rg	3.1100		KDB
ΔfH°gas	[-318.00; -315.30]	kJ/mol
ΔfH°gas	-315.80	kJ/mol	ChemSep v8.3 pure component data Compiled value
ΔfH°gas	-315.30	kJ/mol	KDB
ΔfH°gas	-315.30 ± 0.80	kJ/mol	NIST
ΔfH°gas	-318.00 ± 2.00	kJ/mol	NIST
ΔfH°liquid	[-355.13; -353.50]	kJ/mol
ΔfH°liquid	-355.13 ± 0.86	kJ/mol	NIST
ΔfH°liquid	-353.50 ± 0.80	kJ/mol	NIST
ΔfusH°	12.84	kJ/mol	Joback Calculated Property
ΔvapH°	[34.10; 39.80]	kJ/mol
ΔvapH°	35.56	kJ/mol	NCMS SOLV-DB
ΔvapH°	38.66	kJ/mol	NIST
ΔvapH°	38.64 ± 0.05	kJ/mol	NIST
ΔvapH°	39.80	kJ/mol	NIST
ΔvapH°	38.60 ± 0.10	kJ/mol	NIST
ΔvapH°	35.50	kJ/mol	NIST
ΔvapH°	34.10	kJ/mol	NIST
ΔvapH°	37.49	kJ/mol	NIST
IE	[9.13; 9.43]	eV
IE	9.19 ± 0.01	eV	NIST
IE	9.19 ± 0.01	eV	NIST
IE	9.13 ± 0.03	eV	NIST
IE	9.40	eV	NIST
IE	9.43	eV	NIST
IE	9.41	eV	NIST
IE	9.30 ± 0.10	eV	NIST
IE	9.43	eV	NIST
log10WS	0.27		Relay (1.0) Calculated Property
logPoct/wat	-0.270		NCMS SOLV-DB
McVol	68.100	ml/mol	McGowan Calculated Property
NFPA Fire	3		NCMS SOLV-DB
NFPA Health	2		NCMS SOLV-DB
NFPA Safety	1		NCMS SOLV-DB
Pc	[5000.00; 5471.55]	kPa
Pc	5210.00	kPa	IUPAC Vapor-Liquid Critical Properties of Elements and Compounds, part 7 Compiled value
Pc	5208.11	kPa	PSRK revision IV (2005), critical constants and acentric factors of 1000 components Compiled value
Pc	5170.00	kPa	ChemSep v8.3 pure component data Compiled value
Pc	5210.00	kPa	KDB
Pc	Outlier 5471.55 ± 303.98	kPa	NIST
Pc	5210.00 ± 68.94	kPa	NIST
Pc	5000.00 ± 70.00	kPa	NIST
pKa	-2.92		NCMS SOLV-DB
Ptriple	2.53	kPa	ChemSep v8.3 pure component data Compiled value
ρc	360.35 ± 9.69	kg/m3	NIST
Inp	[643.00; 731.30]
Inp	670.10		NIST
Inp	Outlier 648.00		NIST
Inp	690.00		NIST
Inp	669.70		NIST
Inp	671.00		NIST
Inp	Outlier 731.30		NIST
Inp	718.00		NIST
Inp	Outlier 643.00		NIST
Inp	705.00		NIST
Inp	721.00		NIST
Inp	Outlier 648.00		NIST
Inp	687.00		NIST
Inp	702.00		NIST
Inp	660.30		NIST
Inp	680.00		NIST
Inp	697.00		NIST
Inp	Outlier 651.00		NIST
Inp	687.00		NIST
Inp	690.00		NIST
Inp	696.00		NIST
Inp	696.00		NIST
Inp	698.00		NIST
Inp	694.00		NIST
Inp	690.00		NIST
Inp	692.00		NIST
Inp	693.00		NIST
Inp	696.00		NIST
Inp	699.00		NIST
Inp	690.00		NIST
Inp	696.00		NIST
Inp	696.00		NIST
Inp	697.00		NIST
Inp	680.00		NIST
Inp	694.00		NIST
Inp	694.00		NIST
Inp	705.00		NIST
Inp	690.00		NIST
Inp	702.00		NIST
Inp	690.00		NIST
Inp	696.00		NIST
Inp	706.00		NIST
Inp	692.00		NIST
Inp	686.00		NIST
Inp	687.00		NIST
Inp	690.00		NIST
Inp	692.00		NIST
Inp	670.10		NIST
Inp	Outlier 731.30		NIST
Inp	Outlier 648.00		NIST
Inp	697.00		NIST
Inp	705.00		NIST
Ip	[1065.00; 1105.00]
Ip	1065.00		NIST
Ip	1093.00		NIST
Ip	1097.00		NIST
Ip	1100.00		NIST
Ip	1081.00		NIST
Ip	1065.00		NIST
Ip	1066.00		NIST
Ip	1085.00		NIST
Ip	1105.00		NIST
Ip	1083.00		NIST
Ip	1083.00		NIST
Ip	1068.00		NIST
Ip	1084.00		NIST
Ip	1066.00		NIST
Ip	1065.00		NIST
Ip	1065.00		NIST
Ip	1066.00		NIST
Ip	1083.00		NIST
S°gas	299.91	J/mol×K	NIST
S°liquid	196.60	J/mol×K	NIST
Tboil	[372.00; 375.00]	K
Tboil	374.45	K	Measurement and correlation of binary vapor liquid equilibria of isomeric butanols with 1,4-dioxane
Tboil	374.47	K	Study of isobaric vapour liquid equilibrium of some cyclic ethers with 1-chloropropane: Experimental results and SAFT-VR modelling
Tboil	374.52	K	Vapor-Liquid Equilibrium and Volumetric Measurements for Binary Mixtures of 1,4-Dioxane with Isomeric Chlorobutanes
Tboil	374.50	K	ChemSep v8.3 pure component data Compiled value
Tboil	374.60	K	KDB
Tboil	374.47	K	NCMS SOLV-DB
Tboil	374.20	K	NIST
Tboil	374.00 ± 0.40	K	NIST
Tboil	374.50	K	NIST
Tboil	374.55 ± 0.25	K	NIST
Tboil	374.45	K	NIST
Tboil	374.70 ± 0.30	K	NIST
Tboil	374.40 ± 0.40	K	NIST
Tboil	374.55 ± 0.30	K	NIST
Tboil	374.25 ± 0.20	K	NIST
Tboil	Outlier 372.00 ± 3.00	K	NIST
Tboil	374.15 ± 0.50	K	NIST
Tboil	373.15 ± 1.00	K	NIST
Tboil	375.00 ± 0.20	K	NIST
Tboil	374.65 ± 0.50	K	NIST
Tboil	374.50 ± 0.30	K	NIST
Tboil	374.50 ± 0.30	K	NIST
Tboil	374.15 ± 1.00	K	NIST
Tboil	374.41 ± 0.10	K	NIST
Tboil	374.45 ± 0.30	K	NIST
Tboil	373.40 ± 0.30	K	NIST
Tboil	374.60 ± 0.50	K	NIST
Tboil	373.80 ± 0.50	K	NIST
Tc	[585.15; 588.15]	K
Tc	588.00	K	IUPAC Vapor-Liquid Critical Properties of Elements and Compounds, part 7 Compiled value
Tc	587.00	K	PSRK revision IV (2005), critical constants and acentric factors of 1000 components Compiled value
Tc	587.00	K	ChemSep v8.3 pure component data Compiled value
Tc	587.00	K	KDB
Tc	587.30 ± 1.00	K	NIST
Tc	588.15 ± 2.00	K	NIST
Tc	588.00 ± 2.00	K	NIST
Tc	Outlier 585.15 ± 2.00	K	NIST
Tfus	[278.54; 285.35]	K
Tfus	284.48	K	Efficient determination of crystallisation and melting points at low cooling and heating rates with novel computer controlled equipment
Tfus	284.95	K	Jean-Claude Bradley Open Melting Point Dataset (2014, CC0) Compiled value
Tfus	284.95	K	ChemSep v8.3 pure component data Compiled value
Tfus	284.90	K	KDB
Tfus	284.95	K	NCMS SOLV-DB
Tfus	284.95 ± 0.10	K	NIST
Tfus	284.95	K	NIST
Tfus	Outlier 278.54 ± 0.10	K	NIST
Tfus	284.95 ± 0.05	K	NIST
Tfus	284.95 ± 0.20	K	NIST
Tfus	285.35 ± 0.50	K	NIST
Tfus	285.00 ± 0.20	K	NIST
Tfus	284.70 ± 0.40	K	NIST
Tfus	284.90 ± 0.30	K	NIST
Tfus	284.91 ± 0.30	K	NIST
Tfus	284.95 ± 0.20	K	NIST
Tfus	284.94 ± 0.15	K	NIST
Tfus	284.95 ± 0.20	K	NIST
Tfus	284.15 ± 0.50	K	NIST
Tfus	284.93 ± 0.02	K	NIST
Tfus	283.52 ± 0.20	K	NIST
Tfus	284.80 ± 0.50	K	NIST
Tfus	283.20 ± 0.20	K	NIST
Tfus	283.20 ± 1.50	K	NIST
Ttriple	[284.10; 284.95]	K
Ttriple	284.95	K	ChemSep v8.3 pure component data Compiled value
Ttriple	284.10 ± 0.20	K	NIST
Ttriple	284.10 ± 0.20	K	NIST
UQi	2.28		ChemSep v8.3 pure component data Compiled value
URi	3.07		ChemSep v8.3 pure component data Compiled value
Vc	[0.238; 0.239]	m3/kmol
Vc	0.238	m3/kmol	IUPAC Vapor-Liquid Critical Properties of Elements and Compounds, part 7 Compiled value
Vc	0.238	m3/kmol	PSRK revision IV (2005), critical constants and acentric factors of 1000 components Compiled value
Vc	0.238	m3/kmol	ChemSep v8.3 pure component data Compiled value
Vc	0.238	m3/kmol	KDB
Vc	0.239 ± 0.008	m3/kmol	NIST
Vc	0.239 ± 0.004	m3/kmol	NIST
Zc	[0.2540000; 0.2550000]
Zc	0.2540000		IUPAC Vapor-Liquid Critical Properties of Elements and Compounds, part 7 Compiled value
Zc	0.2550000		ChemSep v8.3 pure component data Compiled value
Zc	0.2540620		KDB
Zra	[0.25; 0.27]
Zra	0.25		ChemSep v8.3 pure component data Compiled value
Zra	0.27		KDB

Temperature Dependent Properties

Property	Value	Unit	Temperature (K)	Source
Cp,liquid	[140.20; 160.40]	J/mol×K	[288.15; 333.15]
Cp,liquid	146.70	J/mol×K	288.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	146.00	J/mol×K	291.00	NIST
Cp,liquid	150.00	J/mol×K	293.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	154.80	J/mol×K	296.00	NIST
Cp,liquid	147.90	J/mol×K	298.00	NIST
Cp,liquid	155.60	J/mol×K	298.00	NIST
Cp,liquid	140.20	J/mol×K	298.00	NIST
Cp,liquid	149.00	J/mol×K	298.00	NIST
Cp,liquid	149.49	J/mol×K	298.15	NIST
Cp,liquid	149.00	J/mol×K	298.15	NIST
Cp,liquid	149.65	J/mol×K	298.15	NIST
Cp,liquid	150.57	J/mol×K	298.15	NIST
Cp,liquid	151.00	J/mol×K	298.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	150.65	J/mol×K	298.15	NIST
Cp,liquid	150.77	J/mol×K	298.15	NIST
Cp,liquid	149.73	J/mol×K	298.15	NIST
Cp,liquid	147.90	J/mol×K	298.15	NIST
Cp,liquid	152.97	J/mol×K	298.20	NIST
Cp,liquid	152.10	J/mol×K	303.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	153.70	J/mol×K	308.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	155.30	J/mol×K	313.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	156.50	J/mol×K	318.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	158.40	J/mol×K	323.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	160.20	J/mol×K	328.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
Cp,liquid	160.40	J/mol×K	333.15	Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
η	[0.0005770; 0.0015900]	Pa×s	[283.15; 353.15]
η	0.0015900	Pa×s	283.15	Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
η	0.0014400	Pa×s	288.15	Viscosity Behavior of Some Oxygen Containing Compounds
η	0.0014381	Pa×s	288.15	Densities and viscosities of binary and ternary mixtures of cyclohexanone, 1,4-dioxane and isooctane from T = (288.15 to 313.15) K
η	0.0013120	Pa×s	293.15	Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
η	0.0013111	Pa×s	293.15	Densities and viscosities of binary and ternary mixtures of cyclohexanone, 1,4-dioxane and isooctane from T = (288.15 to 313.15) K
η	0.0012860	Pa×s	293.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
η	0.0012023	Pa×s	298.15	Densities and viscosities of binary and ternary mixtures of cyclohexanone, 1,4-dioxane and isooctane from T = (288.15 to 313.15) K
η	0.0010870	Pa×s	298.15	NCMS SOLV-DB
η	0.0012236	Pa×s	298.15	Densities, Viscosities, and Sound Speeds of Some Acetate Salts in Binary Mixtures of Tetrahydrofuran and Methanol at (303.15, 313.15, and 323.15) K
η	0.0011780	Pa×s	298.15	Studies on Thermodynamic and Transport Properties of Binary Mixtures of Acetonitrile with Some Cyclic Ethers at Different Temperatures by Volumetric, Viscometric, and Interferometric Techniques
η	0.0011800	Pa×s	298.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
η	0.0011850	Pa×s	298.15	Viscosity Behavior of Some Oxygen Containing Compounds
η	0.0011020	Pa×s	303.15	Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
η	0.0010870	Pa×s	303.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
η	0.0010985	Pa×s	303.15	Viscosities and Densities of Binary Mixtures of 1,4-Dioxane, Carbon Tetrachloride, and Butanol at 303.15 K, 308.15 K, and 313.15 K
η	0.0010983	Pa×s	303.15	Viscosities and Densities of Binary Mixtures of 1,4-Dioxane, Carbon Tetrachloride, and Butanol at 303.15 K, 308.15 K, and 313.15 K
η	0.0011065	Pa×s	303.15	Densities and viscosities of binary and ternary mixtures of cyclohexanone, 1,4-dioxane and isooctane from T = (288.15 to 313.15) K
η	0.0010219	Pa×s	308.15	Densities and viscosities of binary and ternary mixtures of cyclohexanone, 1,4-dioxane and isooctane from T = (288.15 to 313.15) K
η	0.0010290	Pa×s	308.15	Viscosity Behavior of Some Oxygen Containing Compounds
η	0.0009985	Pa×s	308.15	Studies on Thermodynamic and Transport Properties of Binary Mixtures of Acetonitrile with Some Cyclic Ethers at Different Temperatures by Volumetric, Viscometric, and Interferometric Techniques
η	0.0010295	Pa×s	308.15	Viscosities and Densities of Binary Mixtures of 1,4-Dioxane, Carbon Tetrachloride, and Butanol at 303.15 K, 308.15 K, and 313.15 K
η	0.0009268	Pa×s	308.15	Densities, Viscosities, and Sound Speeds of Some Acetate Salts in Binary Mixtures of Tetrahydrofuran and Methanol at (303.15, 313.15, and 323.15) K
η	0.0009477	Pa×s	313.15	Densities and viscosities of binary and ternary mixtures of cyclohexanone, 1,4-dioxane and isooctane from T = (288.15 to 313.15) K
η	0.0009575	Pa×s	313.15	Viscosities and Densities of Binary Mixtures of 1,4-Dioxane, Carbon Tetrachloride, and Butanol at 303.15 K, 308.15 K, and 313.15 K
η	0.0009460	Pa×s	313.15	Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
η	0.0009340	Pa×s	313.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
η	0.0007991	Pa×s	318.15	Densities, Viscosities, and Sound Speeds of Some Acetate Salts in Binary Mixtures of Tetrahydrofuran and Methanol at (303.15, 313.15, and 323.15) K
η	0.0008909	Pa×s	318.15	Studies on Thermodynamic and Transport Properties of Binary Mixtures of Acetonitrile with Some Cyclic Ethers at Different Temperatures by Volumetric, Viscometric, and Interferometric Techniques
η	0.0008140	Pa×s	323.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
η	0.0008250	Pa×s	323.15	Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
η	0.0007180	Pa×s	333.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
η	0.0007210	Pa×s	333.15	Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
η	0.0006400	Pa×s	343.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
η	0.0006400	Pa×s	343.15	Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
η	0.0005770	Pa×s	353.15	Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
σcond	[0.00; 0.00]	S/m	[298.15; 323.15]
σcond	0.00	S/m	298.15	Micellar Properties and Related Thermodynamic Parameters of the 14-6-14, 2Br- Gemini Surfactant in Water + Organic Solvent Mixed Media
σcond	0.00	S/m	303.15	Micellar Properties and Related Thermodynamic Parameters of the 14-6-14, 2Br- Gemini Surfactant in Water + Organic Solvent Mixed Media
σcond	0.00	S/m	315.15	Micellar Properties and Related Thermodynamic Parameters of the 14-6-14, 2Br- Gemini Surfactant in Water + Organic Solvent Mixed Media
σcond	0.00	S/m	323.15	Micellar Properties and Related Thermodynamic Parameters of the 14-6-14, 2Br- Gemini Surfactant in Water + Organic Solvent Mixed Media
ΔfusH	[2.35; 12.84]	kJ/mol	[272.90; 284.10]
ΔfusH	2.35	kJ/mol	272.90	NIST
ΔfusH	11.88	kJ/mol	283.20	NIST
ΔfusH	12.84	kJ/mol	284.10	NIST
ΔfusH	12.84	kJ/mol	284.10	NIST
ΔsubH	35.60	kJ/mol	254.50	NIST
ΔvapH	[34.16; 38.00]	kJ/mol	[273.00; 374.50]
ΔvapH	35.80	kJ/mol	273.00	NIST
ΔvapH	37.00	kJ/mol	318.00	NIST
ΔvapH	38.00	kJ/mol	330.00	NIST
ΔvapH	37.30	kJ/mol	345.50	NIST
ΔvapH	36.50	kJ/mol	350.50	NIST
ΔvapH	34.16	kJ/mol	374.50	NIST
ν	[0.0000009; 0.0000011]	m2/s	[298.15; 313.15]
ν	0.0000011	m2/s	298.15	Experimental and predicted viscosities of binary mixtures of cyclic ethers with 1-chloropentane or 1-chlorohexane at 283.15, 298.15, and 313.15K
ν	0.0000009	m2/s	313.15	Experimental and predicted viscosities of binary mixtures of cyclic ethers with 1-chloropentane or 1-chlorohexane at 283.15, 298.15, and 313.15K
Pvap	[2.38; 19.54]	kPa	[285.11; 328.15]
Pvap	2.38	kPa	285.11	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	2.70	kPa	288.15	Vapor Pressures for 1,4-Dioxane + Tetrabutylammonium Nitrate, Water + Tetrabutylammonium Nitrate, and 1,4-Dioxane + Water + Tetrabutylammonium Nitrate
Pvap	2.92	kPa	288.66	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	3.60	kPa	292.45	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	4.50	kPa	296.56	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	4.50	kPa	296.57	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	4.90	kPa	298.15	Isothermal vapour-liquid equilibrium for cyclic ethers with 1-chloropentane
Pvap	5.08	kPa	298.15	NCMS SOLV-DB
Pvap	4.97	kPa	298.15	Vapor Pressures for 1,4-Dioxane + Tetrabutylammonium Nitrate, Water + Tetrabutylammonium Nitrate, and 1,4-Dioxane + Water + Tetrabutylammonium Nitrate
Pvap	4.90	kPa	298.15	Isothermal (vapour + liquid) equilibrium of (cyclic ethers + chlorohexane) mixtures: Experimental results and SAFT modelling
Pvap	5.34	kPa	299.81	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	6.21	kPa	302.92	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	7.58	kPa	306.93	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	7.57	kPa	306.94	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	8.12	kPa	308.15	Vapor Pressures for 1,4-Dioxane + Tetrabutylammonium Nitrate, Water + Tetrabutylammonium Nitrate, and 1,4-Dioxane + Water + Tetrabutylammonium Nitrate
Pvap	9.19	kPa	311.04	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	10.17	kPa	313.15	Isothermal vapour-liquid equilibrium for cyclic ethers with 1-chloropentane
Pvap	10.29	kPa	313.38	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	10.31	kPa	313.38	Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
Pvap	19.54	kPa	328.15	Isothermal (vapour + liquid) equilibrium of (cyclic ethers + chlorohexane) mixtures: Experimental results and SAFT modelling
Pvap	19.54	kPa	328.15	Isothermal vapour-liquid equilibrium for cyclic ethers with 1-chloropentane
n0	[1.40840; 1.42450]		[288.15; 318.20]
n0	1.42450		288.15	Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
n0	1.42200		293.10	Liquid-Liquid Equilibrium for the System Water + 1,4-Dioxane + 2,6-Dimethyloct-7-en-2-ol over the Temperature Range of (343.2 to 358.2) K
n0	1.42200		293.10	Liquid liquid phase equilibria of the ternary system of water/1,4-dioxane/dihydromyrcene
n0	1.42240		293.15	Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
n0	1.41750		293.15	Solubilities of Phosphorus-Containing Compounds in Selected Solvents
n0	1.41810		298.15	Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of Anisole with 2-Chloroethanol, 1,4-Dioxane, Tetrachloroethylene, Tetrachloroethane, DMF, DMSO, and Diethyl Oxalate at (298.15, 303.15, and 308.15) K
n0	1.42000		298.15	NCMS SOLV-DB
n0	1.42030		298.15	Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
n0	1.42020		298.15	Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethyl Acetoacetate, + Diethyl Oxalate, + Diethyl Phthalate, or + Dioctyl Phthalate at 298.15, 303.15, and 308.15 K
n0	1.41995		298.15	Volumetric and refractive properties of binary mixtures containing 1,4-dioxane and chloroalkanes
n0	1.42020		298.15	Water as a solute in aprotic dipolar solvents. 1. D2O-H2O solute isotope effects on the enthalpy of water dissolution in acetone, tetrahydrofuran and 1,4-dioxane at 298.15 K
n0	1.42030		298.15	Bubble Temperature Measurements on Binary Mixtures Formed by Cyclohexane at 94.7 kPa
n0	1.42010		298.15	Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethanediol, + Hexane, + Tributylamine, or + Triethylamine at (298.15, 303.15, and 308.15) K
n0	1.42030		298.15	Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of 1,4-Dioxane with Different Organic Liquids at (298.15, 303.15, and 308.15) K
n0	1.42010		298.15	Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethyl Acetoacetate, + Diethyl Oxalate, + Diethyl Phthalate, or + Dioctyl Phthalate at 298.15, 303.15, and 308.15 K
n0	1.42000		298.20	A thermodynamic study of solute solvent interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, 1-octanol, and 1,4-dioxane at different temperatures
n0	1.42010		298.20	Dielectric data of binary mixtures of 1,2-butanediol with 2-ethyl-1-hexanol and 1,4-dioxane at T = (298.2, 308.2, and 318.2) K
n0	1.41700		303.15	Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethyl Acetoacetate, + Diethyl Oxalate, + Diethyl Phthalate, or + Dioctyl Phthalate at 298.15, 303.15, and 308.15 K
n0	1.41760		303.15	Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of Anisole with 2-Chloroethanol, 1,4-Dioxane, Tetrachloroethylene, Tetrachloroethane, DMF, DMSO, and Diethyl Oxalate at (298.15, 303.15, and 308.15) K
n0	1.41820		303.15	Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
n0	1.41810		303.15	Thermodynamic Properties of Water + Tetrahydrofuran and Water + 1,4-Dioxane Mixtures at (303.15, 313.15, and 323.15) K
n0	1.41700		303.15	Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethanediol, + Hexane, + Tributylamine, or + Triethylamine at (298.15, 303.15, and 308.15) K
n0	1.41640		303.15	Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of 1,4-Dioxane with Different Organic Liquids at (298.15, 303.15, and 308.15) K
n0	1.41410		308.15	Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of Anisole with 2-Chloroethanol, 1,4-Dioxane, Tetrachloroethylene, Tetrachloroethane, DMF, DMSO, and Diethyl Oxalate at (298.15, 303.15, and 308.15) K
n0	1.41450		308.15	Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of 1,4-Dioxane with Different Organic Liquids at (298.15, 303.15, and 308.15) K
n0	1.41430		308.15	Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethanediol, + Hexane, + Tributylamine, or + Triethylamine at (298.15, 303.15, and 308.15) K
n0	1.41440		308.15	Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethyl Acetoacetate, + Diethyl Oxalate, + Diethyl Phthalate, or + Dioctyl Phthalate at 298.15, 303.15, and 308.15 K
n0	1.41610		308.15	Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
n0	1.41430		308.20	A thermodynamic study of solute solvent interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, 1-octanol, and 1,4-dioxane at different temperatures
n0	1.41440		308.20	A thermodynamic study of solute solvent interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, 1-octanol, and 1,4-dioxane at different temperatures
n0	1.41420		308.20	Dielectric data of binary mixtures of 1,2-butanediol with 2-ethyl-1-hexanol and 1,4-dioxane at T = (298.2, 308.2, and 318.2) K
n0	1.41264		313.15	Volumetric and refractive properties of binary mixtures containing 1,4-dioxane and chloroalkanes
n0	1.41390		313.15	Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
n0	1.41170		318.15	Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
n0	1.40920		318.20	A thermodynamic study of solute solvent interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, 1-octanol, and 1,4-dioxane at different temperatures
n0	1.40840		318.20	Dielectric data of binary mixtures of 1,2-butanediol with 2-ethyl-1-hexanol and 1,4-dioxane at T = (298.2, 308.2, and 318.2) K
n0	1.40840		318.20	A thermodynamic study of solute solvent interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, 1-octanol, and 1,4-dioxane at different temperatures
ρl	[964.63; 1039.12]	kg/m3	[288.15; 353.15]
ρl	1038.78	kg/m3	288.15	Volumetric properties of binary mixtures of ethers and acetonitrile: Experimental results and application of the Prigogine Flory Patterson theory
ρl	1039.12	kg/m3	288.15	Densities and Excess Molar Volumes for the Binary and Ternary Systems of (1,4-Dioxane, 1-Propanol or 2-Propanol, and 1,2-Dichloroethane) at T = (288.15 to 318.15) K. Experimental Measurements and Prigogine-Flory-Patterson Modeling
ρl	1033.00	kg/m3	293.00	KDB
ρl	1033.59	kg/m3	293.15	Thermodynamic Studies of Molecular Interactions in Mixtures Containing Tetrahydropyran, 1,4-dioxane and Cyclic ketones
ρl	1033.57	kg/m3	293.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
ρl	1033.50	kg/m3	293.15	Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
ρl	1033.16	kg/m3	293.15	Volumetric properties of binary mixtures of ethers and acetonitrile: Experimental results and application of the Prigogine Flory Patterson theory
ρl	1033.80	kg/m3	293.15	Volumetric properties of binary mixtures of (water + organic solvents) at temperatures between T = 288.15 K and T = 303.15 K at p = 0.1 MPa
ρl	1027.92	kg/m3	298.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
ρl	1027.86	kg/m3	298.15	Study of intermolecular interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, primary amyl alcohols and 1,4-dioxane at various temperatures
ρl	1027.88	kg/m3	298.15	(Vapour + liquid) equilibrium of binary mixtures (1,3-dioxolane or 1,4-dioxane + 2-methyl-1-propanol or 2-methyl-2-propanol) at isobaric conditions
ρl	1027.51	kg/m3	298.15	Volumetric properties of binary mixtures of ethers and acetonitrile: Experimental results and application of the Prigogine Flory Patterson theory
ρl	1027.85	kg/m3	298.15	Experimental and predicted vapour liquid equilibrium of 1,4-dioxane with cycloalkanes and benzene
ρl	1027.94	kg/m3	298.15	Thermodynamic Studies of Molecular Interactions in Mixtures Containing Tetrahydropyran, 1,4-dioxane and Cyclic ketones
ρl	1027.90	kg/m3	298.15	Densities, Speeds of Sound, Excess Molar Enthalpies, and Heat Capacities of o-Chlorotoluene and Cyclic Ether Mixtures
ρl	1027.85	kg/m3	298.15	Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
ρl	1027.82	kg/m3	298.15	Surface Tension and Surface Properties of Binary Mixtures of 1,4-Dioxane or N,N-Dimethyl Formamide with n-Alkyl Acetates
ρl	1028.20	kg/m3	298.15	Densities, Viscosities, and Sound Speed of Binary Mixtures of Hexyl Acetate with Tetrahydrofuran, 1,4-Dioxane, Anisole, and Butyl Vinyl Ether
ρl	1027.99	kg/m3	298.15	Densities, Viscosities, and Speeds of Sound of Binary Mixtures of Heptan-1-ol with 1,4-Dioxane at Temperatures from (298.15 to 323.15) K and Atmospheric Pressure
ρl	1027.84	kg/m3	298.15	Densities and Excess Molar Volumes for the Binary and Ternary Systems of (1,4-Dioxane, 1-Propanol or 2-Propanol, and 1,2-Dichloroethane) at T = (288.15 to 318.15) K. Experimental Measurements and Prigogine-Flory-Patterson Modeling
ρl	1027.79	kg/m3	298.15	Hydrogen bond interactions in the blends of 1,4-dioxane with some 1, 2- disubstituted ethanes at T = (298.15, 308.15 and 318.15) K
ρl	1027.87	kg/m3	298.15	Surface study of mixtures containing cyclic ethers and isomeric chlorobutanes
ρl	1027.87	kg/m3	298.15	Isothermal Vapor-Liquid Equilibria and Excess Gibbs Energies for Binary Mixtures of Cyclic Ethers with 1,2-Dichloroethane
ρl	1027.90	kg/m3	298.15	Vapour liquid equilibrium of cyclic ethers with 1-chlorohexane: Experimental results and UNIFAC predictions
ρl	1027.89	kg/m3	298.20	Temperature and concentration dependence of the relative permittivity of (1,3-butanediol + 1-octanol or 1,4-dioxane) binary liquid mixtures
ρl	1022.28	kg/m3	303.15	Thermodynamic Studies of Molecular Interactions in Mixtures Containing Tetrahydropyran, 1,4-dioxane and Cyclic ketones
ρl	1022.70	kg/m3	303.15	Densities, Viscosities, and Sound Speed of Binary Mixtures of Hexyl Acetate with Tetrahydrofuran, 1,4-Dioxane, Anisole, and Butyl Vinyl Ether
ρl	1022.30	kg/m3	303.15	Studies of viscosities of dilute solutions of alkylamine in non-electrolyte solvents. II. Haloalkanes and other polar solvents
ρl	1022.30	kg/m3	303.15	Densities, Speeds of Sound, Excess Molar Enthalpies, and Heat Capacities of o-Chlorotoluene and Cyclic Ether Mixtures
ρl	1022.40	kg/m3	303.15	Unravelling various types of non-covalent interactions of benzyl amine with ethers in n-hexane at 303.15 K by ultrasonic and DFT methods
ρl	1022.27	kg/m3	303.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
ρl	1021.84	kg/m3	303.15	Volumetric properties of binary mixtures of ethers and acetonitrile: Experimental results and application of the Prigogine Flory Patterson theory
ρl	1022.19	kg/m3	303.15	Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
ρl	1022.33	kg/m3	303.15	Densities, Viscosities, and Speeds of Sound of Binary Mixtures of Heptan-1-ol with 1,4-Dioxane at Temperatures from (298.15 to 323.15) K and Atmospheric Pressure
ρl	1017.40	kg/m3	308.15	Densities, Viscosities, and Sound Speed of Binary Mixtures of Hexyl Acetate with Tetrahydrofuran, 1,4-Dioxane, Anisole, and Butyl Vinyl Ether
ρl	1016.57	kg/m3	308.15	Densities and Excess Molar Volumes for the Binary and Ternary Systems of (1,4-Dioxane, 1-Propanol or 2-Propanol, and 1,2-Dichloroethane) at T = (288.15 to 318.15) K. Experimental Measurements and Prigogine-Flory-Patterson Modeling
ρl	1016.78	kg/m3	308.15	Hydrogen bond interactions in the blends of 1,4-dioxane with some 1, 2- disubstituted ethanes at T = (298.15, 308.15 and 318.15) K
ρl	1016.60	kg/m3	308.15	Densities, Speeds of Sound, Excess Molar Enthalpies, and Heat Capacities of o-Chlorotoluene and Cyclic Ether Mixtures
ρl	1016.52	kg/m3	308.15	Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
ρl	1016.66	kg/m3	308.15	Densities, Viscosities, and Speeds of Sound of Binary Mixtures of Heptan-1-ol with 1,4-Dioxane at Temperatures from (298.15 to 323.15) K and Atmospheric Pressure
ρl	1016.59	kg/m3	308.15	Thermodynamic Studies of Molecular Interactions in Mixtures Containing Tetrahydropyran, 1,4-dioxane and Cyclic ketones
ρl	1010.91	kg/m3	313.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
ρl	1011.10	kg/m3	313.15	Densities, Viscosities, and Sound Speed of Binary Mixtures of Hexyl Acetate with Tetrahydrofuran, 1,4-Dioxane, Anisole, and Butyl Vinyl Ether
ρl	1010.98	kg/m3	313.15	Densities, Viscosities, and Speeds of Sound of Binary Mixtures of Heptan-1-ol with 1,4-Dioxane at Temperatures from (298.15 to 323.15) K and Atmospheric Pressure
ρl	1010.83	kg/m3	313.15	Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
ρl	1005.12	kg/m3	318.15	Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
ρl	1005.29	kg/m3	318.15	Densities and Excess Molar Volumes for the Binary and Ternary Systems of (1,4-Dioxane, 1-Propanol or 2-Propanol, and 1,2-Dichloroethane) at T = (288.15 to 318.15) K. Experimental Measurements and Prigogine-Flory-Patterson Modeling
ρl	1005.28	kg/m3	318.15	Densities, Viscosities, and Speeds of Sound of Binary Mixtures of Heptan-1-ol with 1,4-Dioxane at Temperatures from (298.15 to 323.15) K and Atmospheric Pressure
ρl	1005.24	kg/m3	318.15	Hydrogen bond interactions in the blends of 1,4-dioxane with some 1, 2- disubstituted ethanes at T = (298.15, 308.15 and 318.15) K
ρl	999.40	kg/m3	323.15	Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
ρl	999.58	kg/m3	323.15	Densities, Viscosities, and Speeds of Sound of Binary Mixtures of Heptan-1-ol with 1,4-Dioxane at Temperatures from (298.15 to 323.15) K and Atmospheric Pressure
ρl	999.49	kg/m3	323.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
ρl	987.97	kg/m3	333.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
ρl	976.37	kg/m3	343.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
ρl	964.63	kg/m3	353.15	Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
D*i	[0.00; 0.00]	m2/s	[288.31; 358.49]
D*i	0.00	m2/s	288.31	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	288.33	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	293.11	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	298.13	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	298.17	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	298.18	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	298.20	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	303.12	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	307.92	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	308.06	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	317.85	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	318.24	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	327.94	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	327.95	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	338.09	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	338.12	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	338.13	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	347.87	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	347.97	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	358.25	Viscous Calibration Liquids for Self-diffusion Measurements
D*i	0.00	m2/s	358.49	Viscous Calibration Liquids for Self-diffusion Measurements
ΔfusS	[8.79; 45.19]	J/mol×K	[272.90; 284.10]
ΔfusS	8.79	J/mol×K	272.90	NIST
ΔfusS	41.90	J/mol×K	283.20	NIST
ΔfusS	45.19	J/mol×K	284.10	NIST
csound,fluid	[1258.60; 1409.60]	m/s	[283.15; 318.15]
csound,fluid	1409.60	m/s	283.15	Speeds of Sound and Isentropic Compressibilities for Binary Mixtures of a Cyclic Diether with a Cyclic Compound at Three Temperatures
csound,fluid	1367.20	m/s	293.15	Physicochemical study of intermolecular interactions in 1,4-dioxane + aromatic hydrocarbons binary mixtures at different temperatures by using ultrasonic and viscometric methods
csound,fluid	1357.70	m/s	295.15	Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
csound,fluid	1343.60	m/s	298.15	Speeds of Sound and Isentropic Compressibilities for Binary Mixtures of a Cyclic Diether with a Cyclic Compound at Three Temperatures
csound,fluid	1344.80	m/s	298.15	Densities and speeds of sound for binary mixtures of (1,3-dioxolane or 1,4-dioxane) with (2-methyl-1-propanol or 2-methyl-2-propanol) at the temperatures 298.15 K and 313.15 K
csound,fluid	1344.70	m/s	298.15	Physicochemical study of intermolecular interactions in 1,4-dioxane + aromatic hydrocarbons binary mixtures at different temperatures by using ultrasonic and viscometric methods
csound,fluid	1344.80	m/s	298.15	Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
csound,fluid	1346.30	m/s	298.15	Compressibility Studies of Binary Solutions Involving Water as a Solute in Nonaqueous Solvents at T ) 298.15 K
csound,fluid	1331.90	m/s	301.15	Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
csound,fluid	1323.10	m/s	303.15	Physicochemical study of intermolecular interactions in 1,4-dioxane + aromatic hydrocarbons binary mixtures at different temperatures by using ultrasonic and viscometric methods
csound,fluid	1319.00	m/s	304.15	Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
csound,fluid	1306.20	m/s	307.15	Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
csound,fluid	1301.20	m/s	308.15	Physicochemical study of intermolecular interactions in 1,4-dioxane + aromatic hydrocarbons binary mixtures at different temperatures by using ultrasonic and viscometric methods
csound,fluid	1293.30	m/s	310.15	Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
csound,fluid	1279.70	m/s	313.15	Physicochemical study of intermolecular interactions in 1,4-dioxane + aromatic hydrocarbons binary mixtures at different temperatures by using ultrasonic and viscometric methods
csound,fluid	1279.80	m/s	313.15	Densities and speeds of sound for binary mixtures of (1,3-dioxolane or 1,4-dioxane) with (2-methyl-1-propanol or 2-methyl-2-propanol) at the temperatures 298.15 K and 313.15 K
csound,fluid	1278.80	m/s	313.15	Speeds of Sound and Isentropic Compressibilities for Binary Mixtures of a Cyclic Diether with a Cyclic Compound at Three Temperatures
csound,fluid	1280.40	m/s	313.15	Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
csound,fluid	1258.60	m/s	318.15	Physicochemical study of intermolecular interactions in 1,4-dioxane + aromatic hydrocarbons binary mixtures at different temperatures by using ultrasonic and viscometric methods
γ	[0.03; 0.04]	N/m	[283.15; 313.15]
γ	0.04	N/m	283.15	Thermophysical study of 1,4-dioxane with cycloalkane mixtures
γ	0.03	N/m	298.15	Thermophysical study of 1,4-dioxane with cycloalkane mixtures
γ	0.03	N/m	298.15	NCMS SOLV-DB
γ	0.03	N/m	313.15	Thermophysical study of 1,4-dioxane with cycloalkane mixtures

Pressure Dependent Properties

Property	Value	Unit	Pressure (kPa)	Source
Tfus(P)	285.08	K	101.30	(Solid + liquid) phase equilibria of binary mixtures containing N-methyl-2-pyrrolidinone and ethers at atmospheric pressure

Datasets

1. Viscosity, Pa*s (2)
2. Mass density, kg/m3 (1)

Viscosity, Pa*s

Fixed		Measured
Temperature, K - Liquid	Pressure, kPa - Liquid	Viscosity, Pa*s - Liquid
303.15	101.33	0.0011
Reference

Fixed		Measured
Temperature, K - Liquid	Pressure, kPa - Liquid	Viscosity, Pa*s - Liquid
303.15	101.30	0.0010
Reference

Mass density, kg/m3

Fixed		Measured
Pressure, kPa - Liquid	Temperature, K - Liquid	Mass density, kg/m3 - Liquid
85.90	298.15	1027.93
Reference

Correlations

Property	Value	Unit	Temperature (K)	Source
Cp,gas	[63.49; 281.92]	J/mol×K	[200.00; 1500.00]	ChemSep v8.3 pure component data Compiled value
Equation			Y = A + exp(B/T + C + D·T + E·T²) Y is Cp,gas in J/mol×K, T in K
Coefficient A			4.62500e+01
Coefficient B			-6.13410e+02
Coefficient C			5.91424e+00
Coefficient D			4.78200e-06
Coefficient E			-2.22380e-08
Temperature range, min.			200.00
Temperature range, max.			1500.00
Cp,gas	63.49	J/mol×K	200.00	Calculated Property
Cp,gas	108.58	J/mol×K	344.44	Calculated Property
Cp,gas	151.52	J/mol×K	488.89	Calculated Property
Cp,gas	185.99	J/mol×K	633.33	Calculated Property
Cp,gas	212.89	J/mol×K	777.78	Calculated Property
Cp,gas	233.90	J/mol×K	922.22	Calculated Property
Cp,gas	250.42	J/mol×K	1066.67	Calculated Property
Cp,gas	263.47	J/mol×K	1211.11	Calculated Property
Cp,gas	273.80	J/mol×K	1355.56	Calculated Property
Cp,gas	281.92	J/mol×K	1500.00	Calculated Property

Property	Value	Unit	Temperature (K)	Source
Cp,liquid	[151.82; 223.75]	J/mol×K	[284.93; 374.47]	ChemSep v8.3 pure component data Compiled value
Equation			Y = A + exp(B/T + C + D·T + E·T²) Y is Cp,liquid in J/mol×K, T in K
Coefficient A			1.51550e+02
Coefficient B			-6.53140e+04
Coefficient C			5.12442e+02
Coefficient D			-1.34020e+00
Coefficient E			1.19890e-03
Temperature range, min.			284.93
Temperature range, max.			374.47
Cp,liquid	151.82	J/mol×K	284.93	Calculated Property
Cp,liquid	152.55	J/mol×K	294.88	Calculated Property
Cp,liquid	154.40	J/mol×K	304.83	Calculated Property
Cp,liquid	158.09	J/mol×K	314.78	Calculated Property
Cp,liquid	164.09	J/mol×K	324.73	Calculated Property
Cp,liquid	172.45	J/mol×K	334.67	Calculated Property
Cp,liquid	182.83	J/mol×K	344.62	Calculated Property
Cp,liquid	194.80	J/mol×K	354.57	Calculated Property
Cp,liquid	208.27	J/mol×K	364.52	Calculated Property
Cp,liquid	223.75	J/mol×K	374.47	Calculated Property

Property	Value	Unit	Temperature (K)	Source
η	[0.0015088; 0.0002308]	Pa×s	[284.95; 487.00]	ChemSep v8.3 pure component data Compiled value
Equation			Y = exp(A + B/T + C·ln(T) + D·T^E) Y is η in Pa×s, T in K
Coefficient A			-7.92800e+01
Coefficient B			4.19840e+03
Coefficient C			1.03930e+01
Coefficient D			-8.55680e-06
Coefficient E			2.00000e+00
Temperature range, min.			284.95
Temperature range, max.			487.00
η	0.0015088	Pa×s	284.95	Calculated Property
η	0.0010097	Pa×s	307.40	Calculated Property
η	0.0007336	Pa×s	329.85	Calculated Property
η	0.0005669	Pa×s	352.30	Calculated Property
η	0.0004588	Pa×s	374.75	Calculated Property
η	0.0003844	Pa×s	397.20	Calculated Property
η	0.0003306	Pa×s	419.65	Calculated Property
η	0.0002897	Pa×s	442.10	Calculated Property
η	0.0002574	Pa×s	464.55	Calculated Property
η	0.0002308	Pa×s	487.00	Calculated Property

Property	Value	Unit	Temperature (K)	Source
ΔvapH	[39.20; 0.00]	kJ/mol	[274.17; 587.00]	ChemSep v8.3 pure component data Compiled value
Equation			Y = A·(1 − Tr)^(B + C·Tr + D·Tr² + E·Tr³), Tr = T/Tc Y is ΔvapH in kJ/mol, T in K
Coefficient A			2.13670e+02
Coefficient B			9.18120e+00
Coefficient C			-2.29920e+01
Coefficient D			2.38540e+01
Coefficient E			-9.34000e+00
Critical temperature, Tc (K)			5.87000e+02
Comment			Range stopped at Tc; ChemSep gives it to 587.56 K.
Temperature range, min.			274.17
Temperature range, max.			587.00
ΔvapH	39.20	kJ/mol	274.17	Calculated Property
ΔvapH	37.57	kJ/mol	308.93	Calculated Property
ΔvapH	36.00	kJ/mol	343.69	Calculated Property
ΔvapH	34.22	kJ/mol	378.45	Calculated Property
ΔvapH	32.05	kJ/mol	413.21	Calculated Property
ΔvapH	29.44	kJ/mol	447.96	Calculated Property
ΔvapH	26.36	kJ/mol	482.72	Calculated Property
ΔvapH	22.67	kJ/mol	517.48	Calculated Property
ΔvapH	17.45	kJ/mol	552.24	Calculated Property
ΔvapH	0.00	kJ/mol	587.00	Calculated Property

Property	Value	Unit	Temperature (K)	Source
Pvap	[1.33; 202.67]	kPa	[274.07; 398.83]	The Yaws Handbook of Vapor Pressure
Equation			ln(Y) = A + B/(T + C) Y is Pvap in kPa, T in K
Coefficient A			1.48111e+01
Coefficient B			-3.42606e+03
Coefficient C			-3.81740e+01
Temperature range, min.			274.07
Temperature range, max.			398.83
Pvap	1.33	kPa	274.07	Calculated Property
Pvap	2.99	kPa	287.93	Calculated Property
Pvap	6.14	kPa	301.79	Calculated Property
Pvap	11.75	kPa	315.66	Calculated Property
Pvap	21.15	kPa	329.52	Calculated Property
Pvap	36.08	kPa	343.38	Calculated Property
Pvap	58.76	kPa	357.24	Calculated Property
Pvap	91.88	kPa	371.11	Calculated Property
Pvap	138.64	kPa	384.97	Calculated Property
Pvap	202.67	kPa	398.83	Calculated Property
Pvap	[2.53; 5170.00]	kPa	[284.95; 580.80]	ChemSep v8.3 pure component data Compiled value
Equation			Y = exp(A + B/T + C·ln(T) + D·T^E) Y is Pvap in kPa, T in K
Coefficient A			4.32073e+01
Coefficient B			-5.57721e+03
Coefficient C			-4.04685e+00
Coefficient D			2.08057e-06
Coefficient E			2.00000e+00
Comment			Range stopped where the equation exceeds Pc; ChemSep gives it to 587 K.
Temperature range, min.			284.95
Temperature range, max.			580.80
Pvap	2.53	kPa	284.95	Calculated Property
Pvap	12.85	kPa	317.82	Calculated Property
Pvap	46.79	kPa	350.69	Calculated Property
Pvap	133.77	kPa	383.57	Calculated Property
Pvap	319.22	kPa	416.44	Calculated Property
Pvap	663.44	kPa	449.31	Calculated Property
Pvap	1238.47	kPa	482.18	Calculated Property
Pvap	2124.21	kPa	515.05	Calculated Property
Pvap	3405.39	kPa	547.93	Calculated Property
Pvap	5170.00	kPa	580.80	Calculated Property
Pvap	[1.26; 5195.37]	kPa	[275.00; 587.00]	KDB Vapor Pressure Data
Equation			ln(Y) = A + B/T + C·ln(T) + D·T² + E/T² Y is Pvap in kPa, T in K
Coefficient A			7.69176e+01
Coefficient B			-7.07594e+03
Coefficient C			-9.15152e+00
Coefficient D			5.90158e-06
Coefficient E			0.00000e+00
Temperature range, min.			275.00
Temperature range, max.			587.00
Pvap	1.26	kPa	275.00	Calculated Property
Pvap	8.54	kPa	309.67	Calculated Property
Pvap	36.89	kPa	344.33	Calculated Property
Pvap	116.49	kPa	379.00	Calculated Property
Pvap	294.01	kPa	413.67	Calculated Property
Pvap	630.26	kPa	448.33	Calculated Property
Pvap	1197.33	kPa	483.00	Calculated Property
Pvap	2078.30	kPa	517.67	Calculated Property
Pvap	3370.87	kPa	552.33	Calculated Property
Pvap	5195.37	kPa	587.00	Calculated Property
Pvap	[3.82; 112.90]	kPa	[293.00; 378.00]	NIST
Equation			ln(Y) = A + B/(T + C) Y is Pvap in kPa, T in K
Coefficient A			1.51541e+01
Coefficient B			-3.61527e+03
Coefficient C			-3.12970e+01
Reference			Crenshaw, Cope, et al., 1938
Comment			Coefficents calculated by NIST from author's data.
Temperature range, min.			293.00
Temperature range, max.			378.00
Pvap	3.82	kPa	293.00	Calculated Property
Pvap	6.18	kPa	302.44	Calculated Property
Pvap	9.68	kPa	311.89	Calculated Property
Pvap	14.72	kPa	321.33	Calculated Property
Pvap	21.81	kPa	330.78	Calculated Property
Pvap	31.54	kPa	340.22	Calculated Property
Pvap	44.64	kPa	349.67	Calculated Property
Pvap	61.91	kPa	359.11	Calculated Property
Pvap	84.31	kPa	368.56	Calculated Property
Pvap	112.90	kPa	378.00	Calculated Property

Property	Value	Unit	Temperature (K)	Source
ρl	[1056.31; 341.16]	kg/m3	[273.83; 587.00]	ChemSep v8.3 pure component data Compiled value
Equation			Y = A / B^(1 + (1 − T/C)^D) Y is ρl in kg/m3, T in K
Coefficient A			8.84487e+01
Coefficient B			2.59260e-01
Coefficient C			5.87000e+02
Coefficient D			2.82780e-01
Temperature range, min.			273.83
Temperature range, max.			587.00
ρl	1056.31	kg/m3	273.83	Calculated Property
ρl	1017.92	kg/m3	308.63	Calculated Property
ρl	977.51	kg/m3	343.42	Calculated Property
ρl	934.59	kg/m3	378.22	Calculated Property
ρl	888.44	kg/m3	413.02	Calculated Property
ρl	837.93	kg/m3	447.81	Calculated Property
ρl	781.12	kg/m3	482.61	Calculated Property
ρl	714.08	kg/m3	517.41	Calculated Property
ρl	626.10	kg/m3	552.20	Calculated Property
ρl	341.16	kg/m3	587.00	Calculated Property

Property	Value	Unit	Temperature (K)	Source
γ	[0.03; 0.02]	N/m	[284.95; 374.35]	Jasper (1972), surface tension of pure liquid compounds Compiled value
Equation			Y = A + B·T + C·T² + D·T³ + E·T⁴ Y is γ in N/m, T in K
Coefficient A			7.42252e-02
Coefficient B			-1.39100e-04
Coefficient C			0.00000e+00
Coefficient D			0.00000e+00
Coefficient E			0.00000e+00
Temperature range, min.			284.95
Temperature range, max.			374.35
γ	0.03	N/m	284.95	Calculated Property
γ	0.03	N/m	294.88	Calculated Property
γ	0.03	N/m	304.82	Calculated Property
γ	0.03	N/m	314.75	Calculated Property
γ	0.03	N/m	324.68	Calculated Property
γ	0.03	N/m	334.62	Calculated Property
γ	0.03	N/m	344.55	Calculated Property
γ	0.02	N/m	354.48	Calculated Property
γ	0.02	N/m	364.42	Calculated Property
γ	0.02	N/m	374.35	Calculated Property
γ	[0.04; 6.17e-06]	N/m	[274.86; 581.38]	ChemSep v8.3 pure component data Compiled value
Equation			Y = A + exp(B/T + C + D·T + E·T²) Y is γ in N/m, T in K
Coefficient A			-1.53900e-02
Coefficient B			-2.37840e+02
Coefficient C			-6.81290e-01
Coefficient D			-5.09840e-03
Coefficient E			-3.52470e-07
Comment			Range stopped where the equation turns negative; ChemSep gives it to 587 K.
Temperature range, min.			274.86
Temperature range, max.			581.38
γ	0.04	N/m	274.86	Calculated Property
γ	0.03	N/m	308.92	Calculated Property
γ	0.03	N/m	342.98	Calculated Property
γ	0.02	N/m	377.03	Calculated Property
γ	0.02	N/m	411.09	Calculated Property
γ	0.01	N/m	445.15	Calculated Property
γ	0.01	N/m	479.21	Calculated Property
γ	0.01	N/m	513.27	Calculated Property
γ	0.00	N/m	547.32	Calculated Property
γ	6.17e-06	N/m	581.38	Calculated Property

Property	Value	Unit	Temperature (K)	Source
λgas	[0.01; 0.06]	W/m×K	[284.95; 768.01]	ChemSep v8.3 pure component data Compiled value
Equation			Y = A·T^B / (1 + C/T + D/T²) Y is λgas in W/m×K, T in K
Coefficient A			2.38730e-07
Coefficient B			1.85050e+00
Coefficient C			-9.45750e+01
Coefficient D			7.80420e+03
Temperature range, min.			284.95
Temperature range, max.			768.01
λgas	0.01	W/m×K	284.95	Calculated Property
λgas	0.01	W/m×K	338.62	Calculated Property
λgas	0.02	W/m×K	392.30	Calculated Property
λgas	0.02	W/m×K	445.97	Calculated Property
λgas	0.03	W/m×K	499.64	Calculated Property
λgas	0.03	W/m×K	553.32	Calculated Property
λgas	0.04	W/m×K	606.99	Calculated Property
λgas	0.05	W/m×K	660.66	Calculated Property
λgas	0.05	W/m×K	714.34	Calculated Property
λgas	0.06	W/m×K	768.01	Calculated Property

Property	Value	Unit	Temperature (K)	Source
λliquid	[0.16; 0.13]	W/m×K	[284.95; 374.47]	ChemSep v8.3 pure component data Compiled value
Equation			Y = A + exp(B/T + C + D·T + E·T²) Y is λliquid in W/m×K, T in K
Coefficient A			8.98340e-02
Coefficient B			4.64210e+01
Coefficient C			-1.18980e+00
Coefficient D			-3.73380e-03
Coefficient E			-6.13580e-06
Temperature range, min.			284.95
Temperature range, max.			374.47
λliquid	0.16	W/m×K	284.95	Calculated Property
λliquid	0.16	W/m×K	294.90	Calculated Property
λliquid	0.15	W/m×K	304.84	Calculated Property
λliquid	0.15	W/m×K	314.79	Calculated Property
λliquid	0.14	W/m×K	324.74	Calculated Property
λliquid	0.14	W/m×K	334.68	Calculated Property
λliquid	0.14	W/m×K	344.63	Calculated Property
λliquid	0.13	W/m×K	354.58	Calculated Property
λliquid	0.13	W/m×K	364.52	Calculated Property
λliquid	0.13	W/m×K	374.47	Calculated Property

Similar Compounds

Find more compounds similar to 1,4-Dioxane.

Mixtures

• Propylamine + 1,4-Dioxane
• 1-Butanamine + 1,4-Dioxane
• 1-Propanamine, N-propyl- + 1,4-Dioxane
• 1-Butanamine, N-butyl- + 1,4-Dioxane
• Triethylamine + 1,4-Dioxane
• 1-Propanamine, N,N-dipropyl- + 1,4-Dioxane
• Tributylamine + 1,4-Dioxane
• 2-Naphthalenecarboxaldehyde + Phthalic anhydride + 1,4-Dioxane
• 2-Naphthalenecarboxaldehyde + 1,4-Dioxane
• Phthalic anhydride + 1,4-Dioxane
• 1,4-Dioxane + Water
• p-Xylene + 1,4-Dioxane
• Benzene, 1,3-dimethyl- + 1,4-Dioxane
• Benzene + BENZENAMINE, 2-METHYL- + 1,4-Dioxane
• Toluene + BENZENAMINE, 2-METHYL- + 1,4-Dioxane
• Benzene, 1,3-dimethyl- + BENZENAMINE, 2-METHYL- + 1,4-Dioxane
• p-Xylene + BENZENAMINE, 2-METHYL- + 1,4-Dioxane
• 1,4-Dioxane + Benzoic acid, 2-methyl-3-nitro-
• Butane, 1-chloro- + 1,4-Dioxane
• Butane, 2-chloro- + 1,4-Dioxane

Find more mixtures with 1,4-Dioxane.

Sources

• KDB Vapor Pressure Data
• Jean-Claude Bradley Open Melting Point Dataset (2014, CC0) ChEDL chemicals 1.5.2, from Bradley, J.-C.; Williams, A.; Lang, A. Jean-Claude Bradley Open Melting Point Dataset. Figshare, 2014 (CC0).
• IUPAC Vapor-Liquid Critical Properties of Elements and Compounds, part 7 ChEDL chemicals 1.5.2, from Kudchadker, A. P.; Ambrose, D.; Tsonopoulos, C. Vapor-Liquid Critical Properties of Elements and Compounds. 7. Oxygen Compounds Other Than Alkanols and Cycloalkanols. J. Chem. Eng. Data 2001, 46, 457-479.
• Jasper (1972), surface tension of pure liquid compounds ChEDL chemicals 1.5.2, from Jasper, J. J. The Surface Tension of Pure Liquid Compounds. J. Phys. Chem. Ref. Data 1972, 1, 841-1010 (as transcribed in Lange's Handbook).
• PSRK revision IV (2005), critical constants and acentric factors of 1000 components ChEDL chemicals 1.5.2, from Horstmann, S.; Jabłoniec, A.; Krafczyk, J.; Fischer, K.; Gmehling, J. PSRK Group Contribution Equation of State: Comprehensive Revision and Extension IV, Including Critical Constants and α-Function Parameters for 1000 Components. Fluid Phase Equilib. 2005, 227, 157-164.
• Cheméo Relay (1.0)
• ChemSep v8.3 pure component data Converted from ChemSep v8.3 pure component data, H. Kooijman and R. Taylor (2021, 2022), Artistic License 2.0; see how the values differ.
• Crippen Method
• Speeds of Sound and Isentropic Compressibilities for Binary Mixtures of a Cyclic Diether with a Cyclic Compound at Three Temperatures
• Viscosity Behavior of Some Oxygen Containing Compounds
• Studies on Hydrogen-Bond Interactions in Ternary Mixtures of Polar Solvents by Dielectric Constant Measurements
• (Solid + liquid) phase equilibria of binary mixtures containing N-methyl-2-pyrrolidinone and ethers at atmospheric pressure
• Solubility of 9-fluorenone, thianthrene and xanthene in organic solvents
• Experimental and predicted vapour liquid equilibrium of 1,4-dioxane with cycloalkanes and benzene
• Experimental and predicted excess molar enthalpies for 1,4-dioxane + octane + cyclohexane at 303.15 K
• Isothermal vapour-liquid equilibrium for cyclic ethers with 1-chloropentane
• Liquid liquid equilibria and partitioning in organic aqueous systems
• Vapour liquid equilibrium of cyclic ethers with 1-chlorohexane: Experimental results and UNIFAC predictions
• Temperature dependence of limiting activity coefficients and Henry s law constants of cyclic and open-chain ethers in water
• Measurement and correlation of binary vapor liquid equilibria of isomeric butanols with 1,4-dioxane
• Study of isobaric vapour liquid equilibrium of some cyclic ethers with 1-chloropropane: Experimental results and SAFT-VR modelling
• Liquid liquid phase equilibria of the ternary system of water/1,4-dioxane/dihydromyrcene
• Density and refractive index measurements of critical mixture 1,4-dioxane + water + saturated KCl in homogenous phase region
• Solubility and preferential solvation of indomethacin in 1,4-dioxane + water solvent mixtures
• Solubility of citric, malonic, and malic acids in different solvents from 303.2 to 333.2 K
• Liquid-liquid equilibrium for the system water + 1,4-dioxane + cyclohexanol over the temperature range of 313.2 - 343.2 K
• Solid-liquid equilibrium (SLE) of ternary system 3-nitrophthalic acid + 4-nitrophthalic acid + 1,4-dioxane at (283.15, 293.15, 303.15, 313.15 and 323.15) K
• Effect of solvent on the volumetric behavior ofN,N' -salicylidenephenyl diamine (Salophen) Schiff base at differenttemperatures (288.15 - 318.15) K
• Study of interaction between organic compounds and mono or dicationic oxygenated ionic liquids using gas chromatography
• Solubility temperature dependence and preferential solvation of sulfadiazine in 1,4-dioxane + water co-solvent mixtures
• Hydrogen bond interactions in the blends of 1,4-dioxane with some 1, 2- disubstituted ethanes at T = (298.15, 308.15 and 318.15) K
• Activity coefficients at infinite dilution of organic solvents and water in 1-butyl-3-methylimidazolium dicyanamide. A literature review of hexane/hex-1-ene separation
• Measurement of the solubility of the salt of 2- mercaptobenzothiazole with cyclohexylamine and tert-butylamine in various solvents at low temperatures: Models and thermodynamic parameters
• High selective water/butan-1-ol separation on investigation of limiting activity coefficients with [P8,8,8,8][[NTf2] ionic liquid
• Separation of binary mixtures based on limiting activity coefficients data using specific ammonium-based ionic liquid and modelling of thermodynamic functions
• Solubility of 1,1-diamino-2,2-dinitroethylene in different pure solvents and binary mixtures (dimethyl sulfoxide p water) and (N,N-dimethylformamide p water) at different temperatures
• Thermodynamics and activity coefficients at infinite dilution for organic solutes in the ionic liquid 1-butyl-1-methylpyrrolidinium dicyanamide
• New ionic liquid [P4,4,4,4][NTf2] in bio-butanol extraction on investigation of limiting activity coefficients
• Unravelling various types of non-covalent interactions of benzyl amine with ethers in n-hexane at 303.15 K by ultrasonic and DFT methods
• Ammonium ionic liquids in extraction of bio-butan-1-ol from water phase using activity coefficients at infinite dilution
• Solubility measurements and thermodynamic modeling of pyrazinamide in five different solvent-antisolvent mixtures
• (Vapour + liquid) equilibrium of binary mixtures (1,3-dioxolane or 1,4-dioxane + 2-methyl-1-propanol or 2-methyl-2-propanol) at isobaric conditions
• Excess molar enthalpies of ternary mixtures of (methanol, ethanol + 2-propanol + 1,4-dioxane) at T ? 298:15 K
• Densities and speeds of sound for binary mixtures of (1,3-dioxolane or 1,4-dioxane) with (2-methyl-1-propanol or 2-methyl-2-propanol) at the temperatures 298.15 K and 313.15 K
• Volumetric properties of binary mixtures of (water + organic solvents) at temperatures between T = 288.15 K and T = 303.15 K at p = 0.1 MPa
• Thermophysical study of 1,4-dioxane with cycloalkane mixtures
• Volumetric and refractive properties of binary mixtures containing 1,4-dioxane and chloroalkanes
• Thermochemical behavior of crown ethers in the mixtures of water with organic solvents. Part VIII. Hydrophobic hydration and preferential solvation of 1,4-dioxane in {(1 - x)amide + xH2O} at T = 298.15 K
• Isothermal compressibility and internal pressure studies of some non-electrolytes in aqueous solutions at low temperatures
• Surface study of mixtures containing cyclic ethers and isomeric chlorobutanes
• Determination of solvation and specific interaction enthalpies of adamantane derivatives in aprotic solvents
• Measurement of activity coefficients at infinite dilution in 1-hexadecyl-3-methylimidazolium tetrafluoroborate ionic liquid
• Apparent molar volumes and apparent molar heat capacities of aqueous tetrahydrofuran, dimethyl sulfoxide, 1,4-dioxane, and 1,2-dimethoxyethane at temperatures from 278.15 K to 393.15 K and at the pressure 0.35 MPa
• Volumetric properties of binary mixtures of ethers and acetonitrile: Experimental results and application of the Prigogine Flory Patterson theory
• Isothermal (vapour + liquid) equilibrium of (cyclic ethers + chlorohexane) mixtures: Experimental results and SAFT modelling
• Efficient determination of crystallisation and melting points at low cooling and heating rates with novel computer controlled equipment
• Thermochemical behaviour of crown ethers in the mixtures of water with organic solvents. Part IX. Effect of base acid properties of {(1 x)AN + xH2O} on the solution enthalpy of cyclic ethers in this mixed solvent at T = 298.15 K
• Thermodynamic properties of solvation of aromatic compounds in cyclohexane, heptane, benzene, 1,4-dioxane, and chloroform at 298.15 K
• Partial molar volumes of organic solutes in water. XXI: Cyclic ethers at temperatures T = (278 to 373) K and at low pressure
• Partial molar volumes of organic solutes in water. XXII. Cyclic ethers at temperatures (298 to 573) K and pressures up to 30 MPa
• Dielectric properties of binary mixtures of three butanediols with 1,4-dioxane and 2-ethyl-1-hexanol at T = 298.2 K
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(3-hydroxypropyl)pyridinium bis(trifluoromethylsulfonyl)-amide
• Solubility and phase separation of 4-morpholinepropanesulfonic acid (MOPS), and 3-morpholino-2-hydroxypropanesulfonic acid (MOPSO) in aqueous 1,4-dioxane and ethanol solutions
• Dielectric data of binary mixtures of 1,2-butanediol with 2-ethyl-1-hexanol and 1,4-dioxane at T = (298.2, 308.2, and 318.2) K
• Solubilities of some organic solutes in 1-ethyl-3-methylimidazolium acetate. Chromatographic measurements and predictions from COSMO-RS
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 4-(2-methoxyethyl)-4-methylmorpholinium bis(trifluoromethylsulfonyl)-amide
• Measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-hexyl-3-methylimidazolium tetracyanoborate
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)-1-methylpiperidinium bis(trifluoromethylsulfonyl)-amide
• Measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-ethyl-3-methylimidazolium methanesulfonate
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)-amide
• Densities and viscosities of binary and ternary mixtures of cyclohexanone, 1,4-dioxane and isooctane from T = (288.15 to 313.15) K
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 4-(2-methoxyethyl)-4-methylmorpholinium trifluorotris(perfluoroethyl)phosphate
• A thermodynamic study of solute solvent interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, 1-octanol, and 1,4-dioxane at different temperatures
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)- 1-methylpiperidinium trifluorotris(perfluoroethyl)phosphate
• Henry s constants and activity coefficients of some organic solutes in 1-butyl,3-methylimidazolium hydrogen sulfate and in 1-methyl,3-trimethylsilylmethylimidazolium chloride
• Physicochemical properties and activity coefficients at infinite dilution for organic solutes and water in a novel bicyclic guanidinium superbase-derived protic ionic liquid
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-methoxyethyl)- 1-methylpyrrolidinium trifluorotris(perfluoroethyl)phosphate
• Measurements of activity coefficients at infinite dilution for organic solutes and water in N-hexylisoquinolinium thiocyanate, [HiQuin][SCN] using GLC
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 1-(2-hydroxyethyl)- 3-methylimidazolium trifluorotris(perfluoroethyl)phosphate
• Temperature and concentration dependence of the relative permittivity of (1,3-butanediol + 1-octanol or 1,4-dioxane) binary liquid mixtures
• Measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-butyl-1-methylpyrrolidinium tricyanomethanide
• Thermodynamics and activity coefficients at infinite dilution for organic solutes and water in the ionic liquid 1-butyl-1-methylmorpholinium tricyanomethanide
• The study of activity coefficients at infinite dilution for organic solutes and water in 1-butyl-4-methylpyridinium dicyanamide, [B4MPy][DCA] using GLC
• Aggregation properties and thermodynamics of micellization of gemini surfactants with diethyl ether spacer in water and water organic solvent mixed media
• Measurement of activity coefficients at infinite dilution of organic solutes in the ionic liquid 1-hexyl-1,4-diaza[2.2.2]bicyclooctanium bis(trifluoromethylsulfonyl)imide using gas-liquid chromatography
• Activity coefficients at infinite dilution of organic solutes in 1-hexyl-3- methylimidazolium trifluoroacetate and influence of interfacial adsorption using gas liquid chromatography
• Experimental and theoretical excess molar properties of imidazolium based ionic liquids with molecular organic solvents I. 1-Hexyl-3- methylimidazlouim tetraflouroborate and 1-octyl-3-methylimidazlouim tetraflouroborate with cyclic ethers
• Thermodynamics and activity coefficients at infinite dilution for organic solutes, water and diols in the ionic liquid choline bis(trifluoromethylsulfonyl)imide
• Solvation parameter model and thermodynamic parameters in a dicationic ionic liquid based on pyrrolidinium
• Experimental and theoretically study of interaction between organic compounds and tricyanomethanide based ionic liquids
• Activity coefficients at infinite dilution of organic solutes in methylphosphonate based ionic liquids using gas-liquid chromatography
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid 4-(3-hydroxypropyl)-4-methylmorpholinium bis(trifluoromethylsulfonyl)-amide
• Activity coefficients at infinite dilution for organic solutes and water in 1-ethyl-1-methylpyrrolidinium lactate
• Activity coefficients at infinite dilution, physicochemical and thermodynamic properties for organic solutes and water in the ionic liquid ethyl-dimethyl-(2-methoxyethyl)ammonium trifluorotris-(perfluoroethyl)phosphate
• Study of intermolecular interactions through dielectric properties of the mixtures consisting of 1,4-butanediol, primary amyl alcohols and 1,4-dioxane at various temperatures
• Solubility of 3-chloro-N-phenylphthalimide in ten organic solvents from T = (288.15 to 323.15) K: Determination and modelling
• A 1-alkylcyanopyridinium-based ionic liquid in the separation processes
• Thermodynamic models for determination of the solubility of 4-(4-aminophenyl)-3-morpholinone in different pure solvents and (1,4-dioxane + ethyl acetate) binary mixtures with temperatures from (278.15 to 333.15) K
• Thermodynamic models for determination of 3-chloro-N-phenylphthalimide solubility in binary solvent mixtures of (acetone, ethyl acetate or 1,4-dioxane + methanol)
• Solubility and solution thermodynamics of 2-methyl-6-nitroaniline in ten organic solvents at elevated temperatures
• Solid-liquid equilibrium and phase diagram for the ternary (2-naphthaldehyde + o-phthalic anhydride + 1,4-dioxane) system
• Viscosity of binary mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid with four organic solvents
• Thermodynamics and selectivity of separation based on activity coefficients at infinite dilution of various solutes in 1-allyl-3-methylimidazolium bis{(trifluoromethyl)sulfonyl}imide ionic liquid
• Thermodynamic study of the solubility of 2,4'-dihydroxydiphenyl sulfone in nine organic solvents from T = (278.15 to 313.15) K and thermodynamic properties of dissolution
• Separation of aliphatic from aromatic hydrocarbons and sulphur compounds from fuel based on measurements of activity coefficients at infinite dilution for organic solutes and water in the ionic liquid N,N-diethyl-N-methyl-N-(2-methoxy-ethyl)ammonium bis(trifluoromethylsulfonyl)imide
• Solubility determination and thermodynamic modeling of 3-methyl-4- nitrobenzoic acid in twelve organic solvents from T = (283.15-318.15) K and mixing properties of solutions
• Measurement and modelling of econazole nitrate in twelve pure organic solvents at temperatures from 278.15 K to 318.15 K
• Solubility determination and thermodynamic modelling of 2,4-dihydro-5-methyl-2-(4-methylphenyl)-3H-pyrazol-3-one in twelve organic solvents from T = (278.15 to 313.15) K and mixing properties of solutions
• Thermodynamics and limiting activity coefficients measurements for organic solutes and water in the ionic liquid 1-dodecyl-3-methylimidzolium bis(trifluoromethylsulfonyl) imide
• Determination and modelling of troxerutin solubility in eleven mono-solvents and (1,4-dioxane + 2-propanol) binary solvents at temperatures from 288.15 K to 323.15 K
• Solubility determination and thermodynamic modelling of 3-amino-1,2,4-triazole in ten organic solvents from T = 283.15 K to T = 318.15 K and mixing properties of solutions
• Solubility measurement, model evaluation and thermodynamic analysis of rivaroxaban polymorphs in organic solvents
• Solubility determination and thermodynamic modeling of paclobutrazol in nine organic solvents from T = (278.15 to 318.15) K and mixing properties of solutions
• Thermodynamic modelling for solubility of 5-chloro-1-methyl-4-nitroimidazole in eleven organic solvents from T = (283.15 to 318.15) K
• Solubility of 3-methyl-4-nitrobenzoic acid in binary solvent mixtures of {(1,4-dioxane, N-methyl-2-pyrrolidone, N,N-dimethylformamide) + methanol} from T = (283.15 to 318.15) K: Experimental determination and thermodynamic modelling
• Thermodynamic study of solubility for 2-amino-4-chloro-6-methoxypyrimidine in twelve organic solvents at temperatures from 273.15 K to 323.15 K
• Solubility determination and modelling of 4-nitro-1,2-phenylenediamine in eleven organic solvents from T = (283.15 to 318.15) K and thermodynamic properties of solutions
• Solubility determination and thermodynamic modelling for 2-amino-4-chlorobenzoic acid in eleven organic solvents from T = (278.15 to 313.15) K and mixing properties of solutions
• Solubility of 2-nitro-p-phenylenediamine in nine pure solvents and mixture of (methanol + N-methyl-2-pyrrolidone) from T = (283.15 to 318.15) K: Determination and modelling
• Physicochemical study of intermolecular interactions in 1,4-dioxane + aromatic hydrocarbons binary mixtures at different temperatures by using ultrasonic and viscometric methods
• Solubility of 4-methyl-2-nitroaniline in fourteen organic solvents from T = (278.15 to 313.15) K and mixing properties of solutions
• Thermodynamic functions for solubility of 3-nitro-o-toluic acid in nine organic solvents from T = (283.15 to 318.15) K and apparent thermodynamic properties of solutions
• Separation of binary mixtures hexane/hex-1-ene, cyclohexane/cyclohexene and ethylbenzene/styrene based on limiting activity coefficients
• Solubility and preferential solvation of econazole nitrate in binary solvent mixtures of methanol, ethanol and 1,4-dioxane in water
• Solubility modelling and dissolution properties of 5-phenyltetrazole in thirteen mono-solvents and liquid mixtures of (methanol + ethyl acetate) at elevated temperatures
• Solubility modelling and preferential solvation of paclobutrazol in cosolvent mixtures of (ethanol, n-propanol and 1,4-dioxane) + water
• Thermodynamic functions for solubility of 2-mercaptobenzothiazole in eleven pure organic solvents at temperatures from 273.15 K to 318.15 K and mixing properties of solutions
• Thermodynamics and activity coefficients at infinite dilution for organic compounds and water in the ionic liquid 1-butyl-3-methylimidazolium perchlorate
• Thermodynamic modelling of solubility and preferential solvation for ribavirin (II) in co-solvent mixtures of (methanol, n-propanol, acetonitrile or 1,4-dioxane) + water
• Separation of water/butan-1-ol based on activity coefficients at infinite dilution in 1,3-didecyl-2-methylimidazolium dicyanamide ionic liquid
• Separation of binary mixtures hexane/hex-1-ene, cyclohexane/cyclohexene and ethylbenzene/styrene based on gamma infinity data measurements
• Separation of binary mixtures based on gamma infinity data using [OMMIM][NTf2] ionic liquid and modelling of thermodynamic functions
• Activity coefficients at infinite dilution and physicochemical properties for organic solutes and water in the ionic liquid trihexyl-tetradecyl-phosphonium tricyanomethanide
• Thermodynamic study of molecular interaction-selectivity in separation processes based on limiting activity coefficients
• Equilibrium solubility and preferential solvation of 1,1'-sulfonylbis(4-aminobenzene) in binary aqueous solutions of n-propanol, isopropanol and 1,4-dioxane
• Abraham model correlations for describing the thermodynamic properties of solute transfer into pentyl acetate based on headspace chromatographic and solubility measurements
• Excess molar volumes and excess isentropic compressibilities of mixtures containing lactam, cyclic ethers and cyclic alkanones
• Thermodynamics and selectivity of separation based on activity coefficients at infinite dilution of various solutes in ionic liquid [HMMIM][BF4]
• The use of ionic liquids for separation of binary hydrocarbons mixtures based on gamma infinity data measurements
• Thermodynamics and activity coefficients at infinite dilution for organic compounds in the ionic liquid 1-hexyl-3-methylimidazolium chloride
• Separation of binary mixtures based on gamma infinity data using [OMMIM][BF4] ionic liquid and modelling of thermodynamic functions
• Equilibrium solubility, solvent effect and preferential solvation of chlorhexidine in aqueous co-solvent solutions of (methanol, ethanol, N,N-dimethylformamide and 1,4-dioxane)
• Determination of the thermodynamic parameters of ionic liquid 1-propyl-3-methylimidazolium bromide by gas-liquid chromatography
• The dissolution behavior and apparent thermodynamic analysis of temozolomide in pure and mixed solvents
• Equilibrium solubility of dinitolmide in several neat solvents and binary aqueous co-solvent mixtures: Experimental determination and thermodynamic analysis
• Equilibrium solubility determination, modelling and thermodynamic aspects of 6-chloroguanine in aqueous co-solvent mixtures of N,N-dimethylformamide, isopropanol, 1,4-dioxane and dimethyl sulfoxide
• Solubility and preferential solvation of flubendazole dissolved in aqueous co-solvent mixtures of 1,4-dioxane, dimethyl sulfoxide, N,N-dimethylformamide and isopropanol
• Vapour-liquid phase boundaries including the near critical regions of the (CO2 + styrene, CO2 + 1,4-dioxane, and CO2 + N,N-dimethylformamide) systems
• The dissolution behaviour and apparent thermodynamic analysis of diprophylline in pure and mixed solvents
• Solubility modelling and thermodynamic aspect of d-aspartic acid in aqueous co-solvent mixtures of N-methyl-2-pyrrolidone, N,N-dimethylformamide, dimethyl sulfoxide and 1.4-dioxane
• Solubility of chloroxine in aqueous co-solvent mixtures of N,N-dimethylformamide, dimethyl sulfoxide, N-methyl-2-pyrrolidone and 1,4-dioxane: Determination, solvent effect and preferential solvation analysis
• Studies of viscosities of dilute solutions of alkylamine in non-electrolyte solvents. II. Haloalkanes and other polar solvents
• Ternary excess molar enthalpies of (1-propanol + 2-propanol + 1,4-dioxane) mixture at 298.15 K
• Thermophysical properties of dimethyl sulfoxide + cyclic and linear ethers at 308.15K Application of an extended cell model
• Experimental and predicted viscosities of binary mixtures of cyclic ethers with 1-chloropentane or 1-chlorohexane at 283.15, 298.15, and 313.15K
• Studies of viscosities of dilute solutions of alkylamines in non-electrolyte solvents: IV. Alkylamines in 1,4-dioxane and oxolane at 303.15K
• Enthalpies of Solution of Glycilglycine in Water-Organic Solvent Media at 298.15 K
• Water as a solute in aprotic dipolar solvents. 1. D2O-H2O solute isotope effects on the enthalpy of water dissolution in acetone, tetrahydrofuran and 1,4-dioxane at 298.15 K
• Excess Molar Enthalpies for Binary and Ternary Mixtures containing Cyclic Ether, 2-Methylaniline and Aromatic Hydrocarbons
• Effect of temperature on the process of preferential solvation of 1,4-dioxane and 12-crown-4 ethers in the mixture of water with formamide
• Solution Enthalpies of 1,4-Dioxane: Study of Solvent Effects Through Quantitative Structure-Property Relationships
• Examination of hydrogen-bonding interactions between dissolved solutes and alkylbenzene solvents based on Abraham model correlations derived from measured enthalpies of solvation
• Use of quantitative structure property relationships to study the solvation process of 18-crown-6
• Influence of the composition of water organic mixtures and the properties of organic solvents on thermochemical characteristics of l-methionine dissolution at 298.15 K
• Effect of halogen substitution on the enthalpies of solvation and hydrogen bonding of organic solutes in chlorobenzene and 1,2-dichlorobenzene derived using multi-parameter correlations
• Thermodynamic of dissolution and hydrogen bond of the pyrrole, N-methylpyrrole with proton acceptors
• Enthalpies of solution and enthalpies of solvation of organic solutes in ethylene glycol at 298.15 K: Prediction and analysis of intermolecular interaction contributions
• Thermochemistry of hydrogen bonding of linear and cyclic amides inproton acceptors media
• Thermochemistry of hydrogen bonding of proton acceptors in the media of linear and cyclic amides. Cooperativity effects in multi-particle complexes of amides
• Solubility and Saturation Apparent Volume of Propranolol Hydrochloride in Some Binary Aqueous Cosolvent Mixtures at 298.15 K
• Solubility of Etoricoxib in Aqueous Solutions of 1,4-Butanediol, 1,4-Dioxane, N,N-Dimethylacetamide, N,N-Dimethylformamide, Dimethyl Sulfoxide, and Ethanol at 298.2 K
• Viscous Calibration Liquids for Self-diffusion Measurements
• Activity Coefficients at Infinite Dilution of Organic Solutes and Water in Tributylethylphosphonium Diethylphosphate Using Gas Liquid Chromatography: Thermodynamic Properties of Mixtures Containing Ionic Liquids
• Solubility Measurement and Thermodynamic Modeling of 4-Nitrophthalimide in Twelve Pure Solvents at Elevated Temperatures Ranging from (273.15 to 323.15) K
• Solubility of 3,7,9,11-Tetraoxo-2,4,6,8,10-pentaaza[3.3.3] Propellane (TOPAP) in Different Pure Solvents at Temperatures between 273.15 and 318.15 K
• Vapor Pressure and Its Temperature Dependence of 28 Organic Compounds: Cyclic Amines, Cyclic Ethers, and Cyclic and Open Chain Secondary Alcohols
• Thermodynamic Studies of Molecular Interactions in Mixtures Containing Tetrahydropyran, 1,4-dioxane and Cyclic ketones
• Solubility Correlation and Thermodynamic Analysis of Sorafenib Free Base and Sorafenib Tosylate in Monosolvents and Binary Solvent Mixtures
• Solubility Measurement and the Correlation of 1-Naphthaleneacetic Acid in Pure and Methanol + Water Binary Solvents from T = (278.25 to 323.55) K
• Thermodynamic Functions for Solubility of 1-Hydroxybenzotriazole in Sixteen Solvents at Temperatures from (278.15 to 313.15) K and Mixing Property of Mixtures
• Solubility Modeling and Mixing Thermodynamics of Thiamphenicol in Water and Twelve Neat Organic Solvents from T = (278.15 to 318.15) K
• Synthesis and Solubility of 5,5-Dimethyl-2-(phenyl(phenylamino)methyl)-1,3,2-dioxaphosphinane 2-oxide in Selected Solvents between 278.15 K and 347.15 K
• Solid-Liquid Equilibrium and Phase Diagram for Ternary 2-Methyl-1,4-naphthoquinone + Phthalic Anhydride +1,4-Dioxane System
• Application of Buffer-Based Ionic Liquid in the Separation of 1,4-Dioxane from Its Azeotropic Aqueous Solution
• Isothermal Vapor-Liquid Equilibria and Excess Gibbs Energies for Binary Mixtures of Cyclic Ethers with 1,2-Dichloroethane
• Solubility of Sulfachloropyridazine in Pure and Binary Solvent Mixtures and Investigation of Intermolecular Interactions
• Densities and Excess Molar Volumes for the Binary and Ternary Systems of (1,4-Dioxane, 1-Propanol or 2-Propanol, and 1,2-Dichloroethane) at T = (288.15 to 318.15) K. Experimental Measurements and Prigogine-Flory-Patterson Modeling
• Determination of Activity Coefficients at Infinite Dilution of Organic Solutes in the Ionic Liquid 1-(2-Hydroxyethyl)-3-methylimidazolium Nonafluoro-1-butanesulfonate Using Gas-Liquid Chromatography
• Solubility Modeling, Solvent Effect, and Preferential Solvation of Thiamphenicol in Cosolvent Mixtures of Methanol, Ethanol, N,N-Dimethylformamide, and 1,4-Dioxane with Water
• Solubility and Molecular Interactions of Trimetazidine Hydrochloride in 12 Monosolvents and Solvent Mixtures of Methanol + (Ethanol, N,N-Dimethylformamide or Ethyl Acetate)
• Solubility Measurement and Modeling of 2-Amino-4,6-dichoropyrimidine in Ten Pure Solvents and (Ethyl Acetate + Ethanol) Solvent Mixtures
• Measurement and Correlation of the Solubility of 5-Fluorouracil in Pure and Binary Solvents
• Solubility Modeling and Solvent Effects of Allopurinol in 15 Neat Solvents
• Thermodynamic Parameters of a New Synthesized Tricationic Ionic Liquid Stationary Phase by Inverse Gas Chromatography
• Solubility Measurement and Thermodynamic Properties of Levetiracetam in Pure and Mixed Solvents
• Measurement and Correlation of Solubility of Gatifloxacin in 12 Pure Solvents from 273.15 K to 318.15 K
• Solubility Measurement and Thermodynamic Model Correlation and Evaluation of 2-Chloro-5-nitroaniline in 12 Pure Solvents
• Solubility Modeling and Solvent Effect of 2-Amino-6-chloropurine in Twelve Neat Solvents
• Solubility in Different Solvents, Correlation, and Solvent Effect in the Solvent Crystallization Process of Iohexol
• Solubility Modeling and Solvent Effect for Flubendazole in 12 Neat Solvents
• Binary Solid-Liquid Solubility Determination and Model Correlation of Quizalofop-p-ethyl in Different Pure Solvents
• Measurement and Correlation of the Solubility of 2-Cyanoacetamide in 14 Pure Solvents and the Mixing Properties of Solutions
• Solubility, Model Correlation, and Solvent Effect of 2-Amino-3-methylbenzoic Acid in 12 Pure Solvents
• Equilibrium Solubility, Model Correlation, and Solvent Effect of Indole-3-acetic Acid in Twelve Pure Solvents
• Solid-Liquid Equilibrium of 5-Chloro-8-hydroxyquinoline and 5,7-Dichloro-8-hydroxyquinoline in Different Solvents and Mixing Properties of Solutions
• Solubility Study of (2E)-1-(3-Pyridyl)-3-(dimethylamino)-2-propen-1-one in Different Pure Solvents and Binary Solvent Mixtures from 278.15 to 328.15 K
• Solubility Determination and Thermodynamic Modeling of 2-Mercaptobenzimidazole in 12 Solvents from T = 278.15 K to T = 318.15 K
• Solubility Determination and Model Correlation of Pymetrozine and Evaluation of the Effect of Solvent Properties and Composition
• Solubility Measurement and Thermodynamic Model Correlation of 5-Nitrosalicylaldehyde in Different Solvents
• o-Nitrophenylacetonitrile Solubility in Several Pure Solvents: Measurement, Correlation, and Solvent Effect Analysis
• Solubility of Gastrodin in Pure and Mixed Solvents at 273.15-313.15 K and Its Correlation with Different Thermodynamic Models
• Solubility and Solvent Effect of Acetamiprid in Thirteen Pure Solvents and Aqueous Solutions of Ethanol
• Solubility Measurement and Correlation of 2-Oxindole in 12 Pure Organic Solvents
• Solubility of d-Aspartic Acid in Several Neat Solvents: Determination, Modeling, and Solvent Effect Analysis
• Densities and Excess Molar Volumes of the Ternary System (1,4-Dioxane + 2-Propanol + 1,1,2,2-Tetrachloroethane) at T = 288.15-318.15 K and at Atmospheric Pressure: Experimental Measurements and Prigogine-Flory-Patterson Modeling
• Solid-Liquid Equilibrium Solubility, Thermodynamic Properties, and Molecular Simulation of Phenylphosphonic Acid in 15 Pure Solvents at Different Temperatures
• Determination and Correlation of Solubilities of 1,3,5-Trifluoro-2,4,6-triiodobenzene in Different Solvents from 289.25 to 332.15 K
• Solubility Determination, Correlation, and Solute-Solvent Molecular Interactions of 5-Aminotetrazole in Various Pure Solvents
• Solubility Determination and Thermodynamic Mixing Properties of 5-Methyl-2-pyrazinecarboxylic Acid in Different Solvents
• Binary Equilibrium Solubility of Amidinothiourea in Monosolvents: Experimental Determination, Model Correlation, and Solvent Effect Analysis
• Measurement and Correlation of Solubility of Marbofloxacin in 12 Pure Solvents from 283.15 to 328.15 K
• Solubility of Acetoguanamine in Twelve Neat Solvents from 283.15 to 323.15 K
• Determination and Modeling of d-Histidine Solubility in Several Pure Solvents from 293.15 to 333.15 K
• Solubility Determination of 2-Chloronicotinic Acid and Analysis of Solvent Effect
• Solubility measurement and thermodynamic model correlation of sancycline in twelve pure solvents
• Solubility and Solution Thermodynamics of 2,6-Dichloro-4-nitroaniline in 12 Pure Solvents at Temperatures from 278.15 to 323.15 K
• Thermodynamic Solubility and Mixing Properties of Phenformin in 14 Pure Solvents at Temperatures Ranging from 278.15 to 323.15 K
• Bubble Temperature Measurements on Binary Mixtures Formed by Cyclohexane at 94.7 kPa
• Vapor-Liquid Equilibrium and Volumetric Measurements for Binary Mixtures of 1,4-Dioxane with Isomeric Chlorobutanes
• Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethanediol, + Hexane, + Tributylamine, or + Triethylamine at (298.15, 303.15, and 308.15) K
• Isothermal Vapor-Liquid Equilibrium Data for the Systems 1,4-Dioxane + Water + Tetrabutylammonium Nitrate and Acetonitrile + Water + Tetrabutylammonium Bromide
• Viscosities and Densities of Binary Mixtures of 1,4-Dioxane, Carbon Tetrachloride, and Butanol at 303.15 K, 308.15 K, and 313.15 K
• Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of 1,4-Dioxane + Ethyl Acetoacetate, + Diethyl Oxalate, + Diethyl Phthalate, or + Dioctyl Phthalate at 298.15, 303.15, and 308.15 K
• Thermodynamic Properties of Water + Tetrahydrofuran and Water + 1,4-Dioxane Mixtures at (303.15, 313.15, and 323.15) K
• Thermodynamics of Mixtures Involving Some Linear or Cyclic Ketones and Cyclic Ethers. 3. Systems Containing 1,4-Dioxane
• Density, Viscosity, and Excess Properties of Binary Liquid Mixtures of Propylene Carbonate with Polar and Nonpolar Solvents
• Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of 1,4-Dioxane with Different Organic Liquids at (298.15, 303.15, and 308.15) K
• Density, Viscosity, Refractive Index, and Speed of Sound for Binary Mixtures of Anisole with 2-Chloroethanol, 1,4-Dioxane, Tetrachloroethylene, Tetrachloroethane, DMF, DMSO, and Diethyl Oxalate at (298.15, 303.15, and 308.15) K
• Excess Molar Enthalpies of Ternary Mixtures of Ethanol + 1-Propanol + Tetrahydropyran or 1,4-Dioxane at 298.15 K
• Thermodynamic Properties of Mixtures Containing Ionic Liquids. 8. Activity Coefficients at Infinite Dilution of Hydrocarbons, Alcohols, Esters, and Aldehydes in 1-Hexyl-3-methylimidazolium Bis(trifluoromethylsulfonyl) Imide Using Gas-Liquid Chromatography
• Determination of Partitioning Coefficients of Numerous Organic Solutes between a Long-Chain Aliphatic Alcohol and the Gas Phase as a Function of Temperature
• Excess Molar Volumes and Viscosity Deviations of Binary Liquid Mixtures of 1,3-Dioxolane and 1,4-Dioxane with Butyl Acetate, Butyric Acid, Butylamine, and 2-Butanone at 298.15 K
• Thermodynamic Properties of Mixtures Containing Ionic Liquids. 9. Activity Coefficients at Infinite Dilution of Hydrocarbons, Alcohols, Esters, and Aldehydes in Trimethyl-butylammonium Bis(trifluoromethylsulfonyl) Imide Using Gas-Liquid Chromatography and Static Method
• Thermodynamic Properties of Mixtures Containing Ionic Liquids: Activity Coefficients at Infinite Dilution of Organic Compounds in 1-Propyl Boronic Acid-3-Alkylimidazolium Bromide and 1-Propenyl-3-alkylimidazolium Bromide Using Inverse Gas Chromatography
• Compressibility Studies of Binary Solutions Involving Water as a Solute in Nonaqueous Solvents at T ) 298.15 K
• Densities, Viscosities, and Sound Speeds of Some Acetate Salts in Binary Mixtures of Tetrahydrofuran and Methanol at (303.15, 313.15, and 323.15) K
• Experimental Study of Thermodynamic Properties of Mixtures Containing Ionic Liquid 1-Ethyl-3-methylimidazolium Ethyl Sulfate Using Gas-Liquid Chromatography and Transpiration Method
• Activity Coefficients at Infinite Dilution of Polar Solutes in 1-Butyl-3-methylimidazolium Tetrafluoroborate Using Gas-Liquid Chromatography
• Studies on Thermodynamic and Transport Properties of Binary Mixtures of Acetonitrile with Some Cyclic Ethers at Different Temperatures by Volumetric, Viscometric, and Interferometric Techniques
• Solubility of Benzoic Acid in Mixed Solvents
• Solubility of 3-Nitrophthalic Acid in Different Solvents between 278 K and 353 K
• Solubilities of Phosphorus-Containing Compounds in Selected Solvents
• Solubility of Form III Piracetam in a Range of Solvents
• Solubilities of N-[(4-Bromo-3,5-difluorine)-phenyl]maleimide in Different Organic Solvents
• Measurement and Correlation for Solubility of 11alpha-Hydroxy-16alpha,17alpha-epoxyprogesterone and 16alpha,17alpha-Epoxyprogesterone in Solvents
• Critical Assessment of CO2 Solubility in Volatile Solvents at 298.15 K
• Solubilities of Phloretin in 12 Solvents at Different Temperatures
• Partial Molar Volumes and Viscosity B-Coefficients of N,N'-Ethylene-bis(salicylideneiminato)cobalt(II) in Binary Mixtures of 1,4-Dioxane + Methanol at T = (298.15, 303.15, 308.15, and 313.15) K
• Activity Coefficients at Infinite Dilution of Organic Compounds in Four New Imidazolium-Based Ionic Liquids
• Solubility and Phase Separation of 2-(N-Morpholino)ethanesulfonic Acid (MES) and 4-(N-Morpholino)butanesulfonic Acid (MOBS) in Aqueous 1,4-Dioxane and Ethanol Solutions
• Partition Coefficients of Organic Compounds in Four New Tetraalkylammonium Bis(trifluoromethylsulfonyl)imide Ionic Liquids Using Inverse Gas Chromatography
• Effect of Base Acid Properties of the Mixture of Water with Propan-1-ol on the Solution Enthalpy of Cyclic Ethers in This Mixture at T = 298.15 K
• Evaluation of the Performance of Trigeminal Tricationic Ionic Liquids for Separation Problems
• Biomass-Derived Platform Chemicals: Thermodynamic Studies on the Extraction of 5-Hydroxymethylfurfural from Ionic Liquids
• Activity Coefficients at Infinite Dilution for Organic Compounds Dissolved in 1-Alkyl-1-methylpyrrolidinium Bis(trifluoromethylsulfonyl)imide Ionic Liquids Having Six-, Eight-, and Ten-Carbon Alkyl Chains
• Solubility of the Metastable Polymorph of Piracetam (Form II) in a Range of Solvents
• Determination of Henry's Law Constants Using Internal Standards with Benchmark Values
• Liquid - Liquid Equilibria for the Ternary Systems of Per fl uorohexane + Methyl Nona fl uorobutyl Ether + Toluene, + 1,4-Dioxane, or + Dimethylformamide at 298.15 K
• Partial Molar Isentropic Compressions of Selected Cyclic Ethers at Infinite Dilution in Water at Temperatures T = (278 to 318) K and Atmospheric Pressure
• Activity Coefficients at Infinite Dilution for Organic Solutes Dissolved in Three 1-Alkyl-1-methylpyrrolidinium Bis(trifluoromethylsulfonyl)imide Ionic Liquids Bearing Short Linear Alkyl Side Chains of Three to Five Carbons
• Solubility Measurement and Modeling for 2-Benzoyl-3-chlorobenzoic Acid and 1-Chloroanthraquinone in Organic Solvents
• Densities, Viscosities, and Speeds of Sound of Binary Mixtures of Heptan-1-ol with 1,4-Dioxane at Temperatures from (298.15 to 323.15) K and Atmospheric Pressure
• Densities, Viscosities, and Sound Speed of Binary Mixtures of Hexyl Acetate with Tetrahydrofuran, 1,4-Dioxane, Anisole, and Butyl Vinyl Ether
• Density and Refractive Index of Binary Mixtures of Two 1-Alkyl-3-methylimidazolium Ionic Liquids with 1,4-Dioxane and Ethylene Glycol
• Densities, Speeds of Sound, Excess Molar Enthalpies, and Heat Capacities of o-Chlorotoluene and Cyclic Ether Mixtures
• Measurement and Correlation of Solubilities of Indole-2-carboxylic Acid in Ten Different Pure Solvents from (278.15 to 360.15) K
• Enthalpies of .beta.-Alanine Dissolution in Some Water + Organic Mixtures at 298.15 K
• Thermodynamics of Fluconazole Solubility in Various Solvents at Different Temperatures
• Infinite Dilution Activity Coefficients of Solutes Dissolved in Two Trihexyl(tetradecyl)phosphonium Ionic Liquids
• Experimental Measurements and Correlations of Excess Molar Enthalpies for the Binary and Ternary Mixtures of (Cyclohexane, 1,4-Dioxane and Piperidine) or (Cyclohexane, Morpholine and Piperidine) at 308.15 K and Atmospheric Pressure
• Measurement of Solid Liquid Phase Equilibrium for the Ternary 3-Nitrophthalic Anhydride + 4-Nitrophthalic Anhydride + 1,4-Dioxane System
• 4-Amino-3,6-dichloropyridazine Solubility Measurement and Correlation in Seven Pure Organic Solvents from (278.15 to 333.15) K
• Solubility and Thermodynamic Functions of Isatin in Pure Solvents
• Determination and Correlation of Solubilities of 2-Isopropylthioxanthone (ITX) in Seven Different Solvents from (299.15 to 329.85) K
• Solubility Determination and Thermodynamic Models for 2-Methylnaphthalene in Different Solvents from T = (278.15 to 303.15) K
• Density, Speed of Sound, and Refractive Index Measurements for the Binary Mixture (1, 4-Dioxane + Isobutyric Acid) at T = (295.15, 298.15, 301.15, 304.15, 307.15, 310.15, and 313.15) K
• Solubility of Irbesartan (Form A) in Different Solvents between 278 K and 323 K
• Densities and Viscosities for Binary and Ternary Mixtures of 1, 4-Dioxane + 1-Hexanol + N,N-Dimethylaniline from T ) (283.15 to 343.15) K
• Solubility of 2-(4-Ethylbenzoyl)benzoic Acid in Eleven Organic Solvents between 279.55 K and 343.15 K
• Ion-Pair and Triple-Ion Formation by Some Tetraalkylammonium Iodides in Binary Mixtures of 1,4-Dioxane + Tetrahydrofuran
• Vapor Pressures for 1,4-Dioxane + Tetrabutylammonium Nitrate, Water + Tetrabutylammonium Nitrate, and 1,4-Dioxane + Water + Tetrabutylammonium Nitrate
• Activity Coefficients at Infinite Dilution of Polar Solutes in 1-Butyl-3-methylimidazolium Trifluoromethanesulfonate Using Gas Liquid Chromatography
• Activity Coefficients at Infinite Dilution of Polar Solutes in 1-Propyl-2,3-dimethylimidazolium Tetrafluoroborate Using Gas Liquid Chromatography
• Salt Effect on the Enthalpy of Mixing of 1,4-Dioxane + Formic Acid at 303.15 K
• Activity Coefficients at Infinite Dilution of Organic Solutes in 1-Ethyl-3-methylimidazolium Tetrafluoroborate Using Gas-Liquid Chromatography
• Solubilities of Salicylic Acid in Pure Solvents and Binary Mixtures Containing Cosolvent
• KCl-Induced Phase Separation of 1,4-Dioxane + Water Mixtures Studied by Electrical Conductivity and Refractive Index
• Densities, Refractive Indices, and Excess Properties of Binary Mixtures of 1,4-Dioxane with Benzene, Toluene, o-Xylene, m-Xylene, p-Xylene, and Mesitylene at Temperatures from (288.15 to 318.15) K
• Activity Coefficients at Infinite Dilution of Organic Compounds in 1-Butyl-3-methylimidazolium Tetrafluoroborate Using Inverse Gas Chromatography
• Activity Coefficients at Infinite Dilution of Organic Compounds in Trihexyl(tetradecyl)phosphonium Bis(trifluoromethylsulfonyl)imide Using Inverse Gas Chromatography
• Solubility of 3-Chlorophthalic Anhydride and 4-Chlorophthalic Anhydride in Organic Solvents and Solubility of 3-Chlorophthalic Acid and 4-Chlorophthalic Acid in Water from (283.15 to 333.15) K
• Excess Molar Enthalpies for the Binary and Ternary Mixtures of Cyclohexane, Tetrahydropyran, and 1,4-Dioxane at 308.15 K and Atmospheric Pressure: Experimental Measurements and Correlations
• Surface Tension and Surface Properties of Binary Mixtures of 1,4-Dioxane or N,N-Dimethyl Formamide with n-Alkyl Acetates
• Partition Coefficients of Organic Compounds in New Imidazolium and Tetralkylammonium Based Ionic Liquids Using Inverse Gas Chromatography
• Transport Properties in 1,4-Dioxane + Water + Saturated KCl Critical Mixture by Measuring Viscosity and Electrical Conductivity
• Liquid-Liquid Equilibrium for the System Water + 1,4-Dioxane + 2,6-Dimethyloct-7-en-2-ol over the Temperature Range of (343.2 to 358.2) K
• Solubility of Biologically Active Chalcones in 1,4-Dioxane and N,N-Dimethyl Formamide from (298.15 to 318.15) K
• Excess Enthalpies of Dibromomethane with Acetone, 1,4-Dioxane, Pyridine, Diethyl Ether, Ethyl Methyl Ketone, and Tetrahydrofuran at 303.15 K
• Activity Coefficients at Infinite Dilution of Polar Solutes in 1-(2-Hydroxyethyl)-3-methylimidazolium Tetrafluoroborate Using Gas-Liquid Chromatography
• Henry s Law Constants of Organic Compounds in Water and n-Octane at T = 293.2 K
• Study of Ether-, Alcohol-, or Cyano-Functionalized Ionic Liquids Using Inverse Gas Chromatography
• Micellar Properties and Related Thermodynamic Parameters of the 14-6-14, 2Br- Gemini Surfactant in Water + Organic Solvent Mixed Media
• Effect of Temperature on the Process of Hydrophobic Hydration. Part I. Hydrophobic Hydration of 1,4-Dioxane and 12-Crown-4 Ethers
• Experimental Measurements and Correlations of Excess Molar Enthalpies for the Binary and Ternary Mixtures of (Cyclohexane, Tetrahydropyran, and Morpholine) or (Cyclohexane, 1,4-Dioxane, and Morpholine) at 308.15 K and Atmospheric Pressure
• Joback Method
• KDB
• McGowan Method
• NIST Webbook
• NCMS SOLV-DB
• The Yaws Handbook of Vapor Pressure

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