SDS Volume

Volume 71. Nitromethane with Water or Organic Solvents, p 1325

Source Publication

Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; Microchem. J. 9, 134-144 (1965).

Conditions:

Room Temp: 297 - 323 $\pu{K}$

Compiler:

V.P. Sazonov

Methodology:

The synthetic method was used. A Reichert microscope, type RCH, equipped with a heating stage was used as described in Schmid, et al. [1]. The disappearance and reappearance of the interface between (1) and (2) could be observed without difficulty.

Sample Information:
  1. Fisher Scientific Co.; certified, No. N-98; $n_{D}^{20}$ = 1.3820, $\rho^{20} = \pu{1134 g L-1}$.
  2. Methyl, ethyl and butyl esters purchased from Applied Science Laboratories; propyl and hexyl esters, formate, propanoate and butyrate prepared by direct esterification; other esters synthesized by transesterification; purified.
Measurement Errors:

Ambient temperature: ±0.5 K.

Methodology Citation

1 Schmid, H. H. O.; Mangold, H. K.; Lundberg, W. O.; J. Am. Oil Chem. Soc. 42, 372 (1965).

System Components:
  1. Nitromethane $\ce{ CH3NO2 }$ [75-52-5]; NIST WebBook
  2. Pentadecylmethanoate $\ce{ C16H32O2 }$ [66271-76-9]; NIST WebBook
    Ethyltetradecanoate $\ce{ C16H32O2 }$ [124-06-1]; NIST WebBook
    Tridecylpropanoate $\ce{ C16H32O2 }$ [6271-77-0]; NIST WebBook
    Dodecylbutanoate $\ce{ C16H32O2 }$ [3724-61-6]; NIST WebBook
    Propyltridecanoate $\ce{ C16H32O2 }$ [88591-28-0]; NIST WebBook
    Butyldodecanoate $\ce{ C16H32O2 }$ [106-18-3]; NIST WebBook
    Decylhexanoate $\ce{ C16H32O2 }$ [52363-43-6]; NIST WebBook
    Hexyldecanoate $\ce{ C16H32O2 }$ [10448-26-7]; NIST WebBook
    Octyloctanoate $\ce{ C16H32O2 }$ [2306-88-9]; NIST WebBook
    Tetradecylethanoate $\ce{ C16H32O2 }$ [638-59-5]; NIST WebBook
    Methyl heptadecanoate $\ce{ C18H36O2 }$ [1731-92-6]; NIST WebBook
Experimental Data

Upper critical solution temperatures of the systems nitromethane (1) with esters (c14) (2)

Esters ($\ce{C16H32O2}$) $T$ (°C) $T$ ($\pu{K}$)
Pentadecylmethanoate (link to XML output link to JSON output link to JSON-LD output) 23.5296.7
Ethyltetradecanoate (link to XML output link to JSON output link to JSON-LD output) 40.5313.7
Tridecylpropanoate (link to XML output link to JSON output link to JSON-LD output) 40.5313.7
Dodecylbutanoate (link to XML output link to JSON output link to JSON-LD output) 44.5317.7
Propyltridecanoate (link to XML output link to JSON output link to JSON-LD output) 45.0318.2
Butyldodecanoate (link to XML output link to JSON output link to JSON-LD output) 47.0320.2
Decylhexanoate (link to XML output link to JSON output link to JSON-LD output) 47.5320.7
Hexyldecanoate (link to XML output link to JSON output link to JSON-LD output) 49.5322.7
Octyloctanoate (link to XML output link to JSON output link to JSON-LD output) 49.5322.7
Tetradecylethanoate (link to XML output link to JSON output link to JSON-LD output) 27.0300.2
Methyl heptadecanoate (link to XML output link to JSON output link to JSON-LD output) 33.5306.7