SDS Volume

Volume 78. Acetonitrile Binary Systems, p 1091

Source Publication

Sedgwick, R. S.; Hoerr, C. W.; Harwood, H. J.; J. Org. Chem. 17, 327 (1952).

Conditions:

Room Temp: 263 - 288 $\pu{K}$

Compiler:

V.P. Sazonov

Methodology:

The synthetic method was used. The solubilities were determined by observing visually the temperature at which crystals appear upon cooling and dissolve upon heating solutions containing known concentrations of solutes. The procedure and equipment were described elsewhere [1].

Sample Information:
  1. Source not specified; best grade; freshly distilled.
  2. Prepared by direct esterification of highly purified fatty acid with the appropriate alcohol; fractionated under a vacuum in a Stedman-packed column; FP = 18.39°C.
Measurement Errors:

Ambient temperature: Not reported.
Mass concentration (m/v) (1): Not reported.

Methodology Citation

1 Hoerr, C. W.; Binkerd, E. F.; Pool, W. O.; Ralston, A. W.; J. Org. Chem. 9, 68-80 (1944).

System Components:
  1. Acetonitrile, $\ce{ C2H3N }$; [75-05-8] NIST WebBook
  2. Methyl tetradecanoate, $\ce{ C15H30O2 }$; [124-10-7] NIST WebBook
Experimental Data

The solubilities of methyl tetradecanoate (2) in acetonitrile (1) in mass percent over the indicated temperature range were reported in graphical form and in a table.

$T$ (°C) $T$ ($\pu{K}$) MR2 (g1/100 g2) 100w2 $x_{2}$
-10.0263.2 <0.1 <0.12 x 10-4
0.0273.2 0.9 9 x 10-32 x 10-3
2.5*275.7 - 0.0163 x 10-3
7.5*280.7 - 0.0509 x 10-3
9.9*283.1 - 0.1000.019
10.0283.2 12.2 0.1090.020
11.3*284.5 - 0.1710.034
11.5*284.7 - 0.2710.059
11.9*285.1 - 0.4350.115
12.5*285.7 - 0.5870.194
13.1*286.3 - 0.7750.368
15.0*288.2 - 0.9120.637

(*) The compiler extracted these data from the published graphs.

Download Data   link to XML output link to JSON output link to JSON-LD output