-
forming diazonium compounds is
called "diazotation", "diazoniation", or "
diazotization". The
reaction was
first reported by
Peter Griess in 1858, who subsequently...
-
sensitive explosive. 1-Diazidocarbamoyl-5-azidotetrazole was
produced by
diazotizing triaminoguanidinium chloride with
sodium nitrite in ultra-purified water...
-
colourless solid is used in
organic synthesis as a
nitrosating agent,
diazotizing agent and a mild oxidant. NOBF4 is the
nitrosonium salt of fluoroboric...
- In chemistry,
amines (/əˈmiːn, ˈæmiːn/, UK also /ˈeɪmiːn/) are
compounds and
functional groups that
contain a
basic nitrogen atom with a lone pair. Formally...
- The
nitrosonium ion is NO+, in
which the
nitrogen atom is
bonded to an
oxygen atom with a bond
order of 3, and the
overall diatomic species bears a positive...
- In
organic chemistry, it is used as a
reagent for nitrosating, as a
diazotizing agent, and as an
oxidizing agent. A
typical procedure entails dissolving...
-
petroleum ether. In the
development of thin
layer chromatography plates with
diazotized p-nitroaniline spray,
cryogenine produces a
purple spot (as does sinicuichine...
- lies at
about 504 nm.: 921
Allura Red AC is
manufactured by
coupling diazotized 5-amino-4-methoxy-2-toluenesulfonic acid with 6-hydroxy-2-naphthalene...
- uses is the
determination of
nitrite in
drinking water. The
Griess diazotization reaction, on
which the
Griess reagent relies, was
first described in...
-
chloride forms green plates[clarification needed]. It can be
readily diazotized, and the
diazonium salt when
boiled with
alcohol yields aposafranine or...
