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IUPAC-NIST Solubility Database
NIST Standard Reference Database 106
Solubility System:
Nitromethane with Hexadecanoic acid
Components:
(1) Hexadecanoic acid; C16H32O2; [57-10-3]
NIST Chemistry WebBook
for detail
(2) Nitromethane; CH3NO2; [75-52-5]
NIST Chemistry WebBook
for detail
Original Measurements:
Broughton, G.; Jones, D.C., Trans. Faraday Soc. 32, 685-9 (1936).
Variables:
Temperature = 366 K to 378 K
Prepared By:
V. P. Sazonov
Experimental Data:
(Notes on the Nomenclature)
Mutual slubility of nitromethane and hexadecanoic acid
t/°C
T/K
10
2
* Mass Fraction w
1
Mole Fraction x
1
(compiler)
Comment(s)
92.40
365.55
27.16
0.6104
Acid-rich phase
92.40
365.55
-
-
Nitromethane-rich phase
94.05
367.20
-
-
Acid-rich phase
94.05
367.20
87.86
0.9682
Nitromethane-rich phase
100.05
373.65
38.20
0.7220
Acid-rich phase
100.05
373.65
-
-
Nitromethane-rich phase
101.60
374.75
-
-
Acid-rich phase
101.60
374.75
81.55
0.9489
Nitromethane-rich phase
101.65
374.80
41.07
0.7454
Acid-rich phase
101.65
374.80
-
-
Nitromethane-rich phase
102.75
375.90
-
-
Acid-rich phase
102.75
375.90
77.10
0.9340
Nitromethane-rich phase
103.55
376.70
46.85
0.7874
Acid-rich phase
103.55
376.70
-
-
Nitromethane-rich phase
103.95
377.10
-
-
Acid-rich phase
103.95
377.10
71.56
0.9136
Nitromethane-rich phase
104.15
377.30
-
-
Acid-rich phase
104.15
377.30
68.03
0.8994
Nitromethane-rich phase
104.30
377.45
-
-
Acid-rich phase
104.30
377.45
66.64
0.8935
Nitromethane-rich phase
104.30
377.45
-
-
Acid-rich phase
104.30
377.45
65.70
0.8895
Nitromethane-rich phase
104.45
377.60
54.23
0.8327
Acid-rich phase
104.45
377.60
-
-
Nitromethane-rich phase
104.50
377.65
61.05
0.8682
Acid-rich phase
104.50
377.65
-
-
Nitromethane-rich phase
104.55
377.70
62.52
0.8751
Acid-rich phase
104.55
377.70
-
-
Nitromethane-rich phase
104.55
377.70
-
-
Acid-rich phase
104.55
377.70
-
- (UCST)
Nitromethane-rich phase
Method/Apparatus/Procedure:
The synthetic method, as described in Broughton,
1
was used. Liquids were pipetted into glass tubes. Temperatures at which complete miscibility occurred were measured by thermometers standardized against a set of thermometers having NPL certificates.
Source and Purity of Materials:
(1) Prepared from sodium monochloroacetate with sodium nitrite; distilled;
n
(25 °C, D) = 1.3796,
d
(25 °C) = 1130.8 g·L
-1
.
(2) Source not specified; purified according to Jones and Betts
2
(recrystallized from petrol ether and ethanol, m. p. = 62.6 °C).
Estimated Errors:
Temperature: ± 0.05 K.
References:
1
G. Broughton, Trans. Faraday Soc. 30, 367 (1934).
2
D. C. Jones and H. F. Betts, J. Chem. Soc. 1177 (1928).