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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.

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