NITRO DERIVATIVES OF HIGHER BENZENE HOMOLOGUES^399
Physical properties of 2,4,6-trinitro-m-xylene
2,4,6-Trinitro-m-xylene crystallizes in white crystals at room temperature.
It is only slightly soluble in concentrated sulphuric acid - at a temperature of
150-160°C 10% of it goes into solution. In fuming sulphuric acid the solubility
is higher.
The solubility of 2,4,6-trinitro-m-xylene in organic solvents is much lower than
that of α− trinitrotoluene (Table 88).
TABLE 88
SOLUBILITY OF 2,4,6-TRINITRO-m-XYLENB IN ORGANIC SOLVENTS
At room temperature At boiling point
Solvent g/100 ml of the solvent g/100 ml of the
solvent
Benzene 0.5 7.5
Toluene 0.5 20.5
Alcohol 0.05 0.55
The solubilities of trinitro-m-xylene (m. p. 180.5°C) in mixtures of benzene with
alcohol (after Kravchinskii [3]) are given below (Table 89).
TABLE 89
SOLUBILITY OFTRINITRO-m-XYLENE IN MIXTURESOF BENZENE
WITH ALCOHOL
Composition of the solvent,
parts by volume
benzene alcohol
1 0.5
1 1
1 1.5
1 2
Solubility, g/100 ml of the
solvents
at 8°C at 20°C
0.71
0.32 0.45
0.24 0.29
- 0.2
At high temperatures 2,4,6-trinitro-m-xylene is readily dissolved by acetic acid
and by aniline. 2,4,6-Trinitro-m-xylene forms eutectics with aromatic hydrocarbons
and their nitro derivatives. Some of the available data are tabulated (Table 90).
The steam volatility of 2,4,6-trinitro-m-xylene is low. At a temperature of 100°C
it begins to sublime. It can be purified by sublimation at 150-170°C. The thermal
conductivity of 2,4,6-trinitro-m-xylene at 25°C is 0.00057 (Prentiss [12]).
chemical properties of 2,4,6-trinitro-m-xylene
2,4,6-Trinitro-m-xylene is not affected by hot concentrated sulphuric and hydro-
chloric acids, but it reacts with alkalis in the presence of alcohol or acetone, yielding
an intense blue addition product.