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Properties of substance:
diphenylamine
Group of substances:
organic
Physical appearance:
white crystals
Empirical formula (Hill's system for organic substances):
C
1
2
H
1
1
N
Structural formula as text:
(C6H5)2NH
Molar/atomic mass: 169.222
Melting point (°C):
54
Boiling point (°C):
302
Solubility (g/100 g of solvent):
1-propanol
: 29.4 (14.5°C) [
Ref.
]
acetone
: 239.83 (0°C) [
Ref.
]
acetone
: 298.59 (28°C) [
Ref.
]
benzene
: 110.674 (0°C) [
Ref.
]
benzene
: 277.99 (28°C) [
Ref.
]
benzene
: 416.67 (40°C) [
Ref.
]
carbon disulphide
: 112.452 (0°C) [
Ref.
]
carbon disulphide
: 314.12 (28°C) [
Ref.
]
carbon tetrachloride
: 27.734 (0°C) [
Ref.
]
carbon tetrachloride
: 122.63 (28°C) [
Ref.
]
chloroform
: 86.545 (0°C) [
Ref.
]
chloroform
: 206.26 (28°C) [
Ref.
]
diethyl ether
: 140.576 (0°C) [
Ref.
]
diethyl ether
: 324.79 (28°C) [
Ref.
]
ethanol abs.
: 26.269 (0°C) [
Ref.
]
ethanol abs.
: 95.842 (28°C) [
Ref.
]
ethanol abs.
: 385.83 (40°C) [
Ref.
]
ethyl acetate
: 135.218 (0°C) [
Ref.
]
ethyl acetate
: 306.79 (28°C) [
Ref.
]
hexane
: 0.5 (-30°C) [
Ref.
]
hexane
: 1.4 (-10°C) [
Ref.
]
hexane
: 2.6 (0°C) [
Ref.
]
hexane
: 6.7 (20°C) [
Ref.
]
hexane
: 13.8 (30°C) [
Ref.
]
hexane
: 94 (50°C) [
Ref.
]
hydrogen fluoride
: very soluble [
Ref.
]
m-xylene
: 49.976 (0°C) [
Ref.
]
m-xylene
: 163.14 (28°C) [
Ref.
]
m-xylene
: 247.85 (40°C) [
Ref.
]
methanol
: 26.708 (0°C) [
Ref.
]
methanol
: 122.98 (28°C) [
Ref.
]
methanol
: 516.55 (40°C) [
Ref.
]
pyridine
: 217.626 (0°C) [
Ref.
]
pyridine
: 306.91 (28°C) [
Ref.
]
pyridine
: 425.62 (40°C) [
Ref.
]
toluene
: 85.794 (0°C) [
Ref.
]
toluene
: 227.65 (28°C) [
Ref.
]
toluene
: 315.72 (40°C) [
Ref.
]
water
: 0.003 (0°C) [
Ref.
]
water
: 0.00316 (15°C) [
Ref.
]
water
: 0.007 (28°C) [
Ref.
]
water
: 0.012 (50°C) [
Ref.
]
water
: 0.032 (85°C) [
Ref.
]
Numerical data:
Year of discovery: 1864
Reactions of synthesis:
Yeild 81%. [
Ref.1
]
C
6
H
5
Cl + C
6
H
5
NH
2
→ C
6
H
5
NHC
6
H
5
+ HCl
Reactions:
Yeild 82-85%. [
Ref.1
]
2(C
6
H
5
)
2
NH + 2C
6
H
5
I + K
2
CO
3
→ 2(C
6
H
5
)
3
N + 2KI + CO
2
+ H
2
O
[
Ref.1
]
(C
6
H
5
)
2
NH + (CH
3
CO)
2
O → CH
3
CON(C
6
H
5
)
2
+ CH
3
COOH
Dissociation:
pK
BH
+
(1) = 0.9 (25°C, water)
LD
50
(mg/kg):
2900 (white mice, oral)
References:
Seidell A. Solubilities of organic compounds. - 3ed., vol.2. - New York: D. Van Nostrand Company, 1941. - pp. 702-705
Горбунов Б.Н., Гурвич Я.А., Маслова И.П. Химия и технология стабилизаторов полимерных материалов. - М.: Химия, 1981. - pp. 46-51 [Russian]
Справочник по растворимости. - Т.1, Кн.1. - М.-Л.: ИАН СССР, 1961. - pp. 516 [Russian]
Справочник по растворимости. - Т.1, Кн.2. - М.-Л.: ИАН СССР, 1962. - pp. 1049, 1148, 1552 [Russian]
Химическая энциклопедия. - Т. 2. - М.: Советская энциклопедия, 1990. - pp. 95 [Russian]
Химический энциклопедический словарь. - Под ред. Кнунянц И.Л. - М.: Советская энциклопедия, 1983. - pp. 184 [Russian]
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© Collected Ruslan Anatolievich Kiper, burewestnik@mail.ru