Glenn T. Hefter
-1
4e-01
Ambient temperature
1
4
°C
1
-5
3.54e-05
Mole fraction - Liquid (1)
3
3.54
1
-2
2.09e-02
Relative mass - solution (1)
3
2.09
g<sub>1</sub>/100 g sln
0
5.2e+00
Ambient temperature
2
5.2
°C
2
-5
3.41e-05
Mole fraction - Liquid (1)
3
3.41
1
-2
2.01e-02
Relative mass - solution (1)
3
2.01
g<sub>1</sub>/100 g sln
1
1.49e+01
Ambient temperature
3
1.49
°C
3
-5
3.25e-05
Mole fraction - Liquid (1)
3
3.25
1
-2
1.92e-02
Relative mass - solution (1)
3
1.92
g<sub>1</sub>/100 g sln
1
2.10e+01
Ambient temperature
3
2.10
°C
4
-5
3.33e-05
Mole fraction - Liquid (1)
3
3.33
1
-2
1.96e-02
Relative mass - solution (1)
3
1.96
g<sub>1</sub>/100 g sln
1
2.50e+01
Ambient temperature
3
2.50
°C
5
-5
3.33e-05
Mole fraction - Liquid (1)
3
3.33
1
-2
1.96e-02
Relative mass - solution (1)
3
1.96
g<sub>1</sub>/100 g sln
1
2.56e+01
Ambient temperature
3
2.56
°C
6
-5
3.33e-05
Mole fraction - Liquid (1)
3
3.33
1
-2
1.96e-02
Relative mass - solution (1)
3
1.96
g<sub>1</sub>/100 g sln
1
3.03e+01
Ambient temperature
3
3.03
°C
7
-5
3.36e-05
Mole fraction - Liquid (1)
3
3.36
1
-2
1.98e-02
Relative mass - solution (1)
3
1.98
g<sub>1</sub>/100 g sln
1
3.49e+01
Ambient temperature
3
3.49
°C
8
-5
3.44e-05
Mole fraction - Liquid (1)
3
3.44
1
-2
2.03e-02
Relative mass - solution (1)
3
2.03
g<sub>1</sub>/100 g sln
1
3.96e+01
Ambient temperature
3
3.96
°C
9
-5
3.69e-05
Mole fraction - Liquid (1)
3
3.69
1
-2
2.18e-02
Relative mass - solution (1)
3
2.18
g<sub>1</sub>/100 g sln
1
Solubility of m-xylene in water
Solubility, Solubility data series
A round-bottomed flask containing about 4 mL of (1) and 400 mL of (2) was evacuated, suspended in a thermostat, shaken for 24h and then allowed to settle for at least another 24h. Next, desired quantities of the water layer were syphoned into 6 glass-stoppered Erlenmeyer flasks. These 6 flasks had previously been tared, partialy filled with a suitable amount of diluent water, and reweighed. Weighed portions of the samples were inserted into a quartz cuvette and measured in a Beckman DU spectrophotometer. Absorbances were corrected for adsorption of (1) onto the walls of the cuvette.
The International Union of Pure and Applied Chemistry
Bohon, R. L.; Claussen, W. F.; J. Am. Chem. Soc. 1951, 73, 1571-8.
paper
https://doi.org/10.1021/ja01148a047
108-38-3
1
C8H10
InChI=1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3
IVSZLXZYQVIEFR-UHFFFAOYSA-N
106.165
1,3-Dimethylbenzene
Oronite Chemical Co. was sulphonated, hydrolysed, steam distilled, washed, dried by passing through silica gel and finally distilled. Purity was judged by refractometry (no value given).
7732-18-5
2
H2O
InChI=1S/H2O/h1H2
XLYOFNOQVPJJNP-UHFFFAOYSA-N
18.0153
Water
Air-free conductivity water (no details given).
m-Xylene with Water
Solubility data from IUPAC SDS Volume 38 (page ?) - m-Xylene with Water