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In this form, it is the salt of a sulfonic acid.
Its sulfonic acid has been detected in the urine of horses and humans.
This sulfonation can be highly specific to place the sulfonic acid group across the ring, in the 4-position.
Taurine is one of the few known naturally occurring sulfonic acids.
This oxidizes the material to a sulfate or sulfonic acid.
A sulfonate is a salt or ester of a sulfonic acid.
Sulfonic acid is produced by the process of sulfonation.
Once the thiols on hair have been oxidized to sulfonic acids, there's really no going back.
During this reaction, nitro groups are introduced, and the sulfonic acid group is displaced.
Since the sulfonic acid was not consumed, it was an early example of a catalyst.
It does contain a sulfonate group and may be called an amino sulfonic acid.
Numerous sulfonic acids derived from 2-naphthylamine are known.
The structure of sulfonic acids is illustrated by the prototype, methanesulfonic acid.
Many other acids are also used such as polymeric sulfonic acids.
Because of their polarity, sulfonic acids tend to be crystalline solids.
It is also known as chlorosulfonic acid, being the sulfonic acid of chlorine.
Because phenylbenzimidazole sulfonic acid is water-soluble, it has the characteristic of feeling lighter on skin.
The nonfluorinated sulfonic acids tend to have low toxicities.
Unlike sulfuric acid itself, sulfonic acids can be solids.
The resulting alkylbenzene compounds are sulfonated to give the corresponding sulfonic acids.
Sulfonic acids are used in many detergents.
One synthetic procedure to synthesize sulfonic acid chlorides is the Reed reaction.
The sulfonic acid is subsequently neutralized with sodium hydroxide.
Hairs with sulfonic acids on them tend to tangle, unless you lubricate them.
Sulfonic acids, which are organic oxyacids, are a class of strong acids.