-
Paraldehyde is the
cyclic trimer of
acetaldehyde molecules. Formally, it is a
derivative of 1,3,5-trioxane, with a
methyl group substituted for a hydrogen...
- 2-Ethoxyethyl
acetate 2-Hydroxyisocaproic acid 4-Hydroxy-4-methylpentanoic acid
Paraldehyde Propylene glycol methyl ether acetate Solketal 9-Crown-3 This set index...
-
stereomers of
paraldehyde and four of metaldehyde. The
German chemist Valentin Hermann Weidenbusch (1821–1893)
synthesized paraldehyde in 1848 by treating...
- The
liquid trimer,
paraldehyde is also obtained. The
reaction is reversible; upon
heating to
about 80 °C,
metaldehyde and
paraldehyde revert to acetaldehyde...
-
stabilizer in many medications; historically, the "P" also
stood for
Paraldehyde,
though this
substance is not
commonly used today) I — Infection, Iron...
- antipsychotics, such as
haloperidol may also be used.
Older drugs such as
paraldehyde and
clomethiazole were
formerly the
traditional treatment but have now...
-
colorless liquid with a
burning flavor and an
unpleasant odor
similar to
paraldehyde with a hint of camphor. TAA
remains liquid at room temperature, making...
- solvent, a.k.a. methylal, a.k.a.
formal [ambiguous]
Dioxolane Metaldehyde Paraldehyde 1,3,5-Trioxane
Phenylsulfonylethylidene (PSE)
acetal is an
example of...
-
Clomethiazole Dichloralphenazone Gaboxadol Kavalactones Loreclezole Paraldehyde Petrichloral Sulfonylalkanes Sulfonmethane (sulfonal)
Tetronal Trional...
- the
dates in
parentheses are the
earliest approved use of the drug.
Paraldehyde (1882). One of the
earliest anticonvulsants. It is
still used to treat...
