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Anthraquinone, also
called anthracenedione or dioxoanthracene, is an
aromatic organic compound with
formula C 14H 8O 2.
Several isomers exist but these...
- For the
parent molecule 9,10-
anthraquinone, see
anthraquinone Anthraquinones (also
known as anthraqui****ids) are a
class of
naturally occurring phenolic...
- The
anthraquinone process, also
called the Riedl–Pfleiderer process, is a
process for the
production of
hydrogen peroxide,
which was
developed by IG Farben...
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examples are 1,2-benzoquinone (ortho-quinone), 1,4-naphthoquinone and 9,10-
anthraquinone. The name is
derived from that of
quinic acid (with the
suffix "-one"...
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Anthraquinone dyes are an
abundant group of dyes
comprising a
anthraquinone unit as the
shared structural element.
Anthraquinone itself is colourless,...
- (casanthranol)
Anthraquinone colon 36–8
hours Buckthorn Anthraquinone colon 36–8
hours Senna extract (senna glycoside)
Anthraquinone colon 36–8 hours...
- 10-
anthraquinone (AQ). It
formed when AQ is hydrogenated. It is
easily dissolved in
alkaline solutions and is
often called soluble anthraquinone (SAQ)...
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polar molecules containing anthraquinone or azo groups. It is
estimated that 85% of dis**** dyes are azos or
anthraquinone dyes. The
history of dis****...
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exclusively by the
anthraquinone process,
which was
originally developed by BASF in 1939. It
begins with the
reduction of an
anthraquinone (such as 2-ethylanthraquinone...
- many
dihydroxy derivatives of
other anthraquinones, such as 1,2-
anthraquinone, 1,4-
anthraquinone, and 2,6-
anthraquinone.
Hydroxyquinone Hydroxybenzoquinone...
