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:
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:
- Fisher Scientific Co.; certified, No. N-98; $n_{D}^{20}$ = 1.3820, $\rho^{20} = \pu{1134 g L-1}$.
- 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:
- Nitromethane $\ce{ CH3NO2 }$ [75-52-5]; NIST WebBook
-
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)


