SDS Volume

Volume 78. Acetonitrile Binary Systems, p 1098

Source Publication

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

Conditions:

Room Temp: 283 - 303 $\pu{K}$

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 = 31.36°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. Ethyl octadecanoate, $\ce{ C20H40O2 }$; [111-61-5] NIST WebBook
Experimental Data
$T$ (°C) $T$ ($\pu{K}$) MR2 (g1/100 g2) 100w2 $x_{2}$
10.0283.2 0.2 2 x 10-33 x 10-4
20.0293.2 1.5 0.0152 x 10-3
30.0303.2 7.2 0.0679 x 10-3

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