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Calcium xylene sulfonate and sodium cumene sulfonate have been shown to cause temporary, slight eye irritation in animals. [9] Studies have not found hydrotropes to be mutagenic, carcinogenic or have reproductive toxicity.
CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA) 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0 C 20 H 25 N 30: Lysergic acid diethylamide (LSD) 50–37–3 C 123 H 193 N 35 O 37: Common serum albumin (macromolecule) 9048–49–1 Ca(AlH 4) 2: calcium ...
An example of a linear alkylbenzene sulfonate (LAS) Linear alkylbenzene sulfonates (LAS) are prepared industrially by the sulfonation of linear alkylbenzenes (LABs), which can themselves be prepared in several ways. [2] In the most common route benzene is alkylated by long chain monoalkenes (e.g. dodecene) using hydrogen fluoride as a catalyst. [9]
The sulfonate group is negative in aqueous solution, which is why the α-olefin sulfonates are among the anionic surfactants. In contrast to most other surfactants in which the C 12 -alkyl chains have the highest surface activity, olefin sulfonates shows maximal activity when using C 14 and C 16 -olefins.
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The sulfonate ion. In organosulfur chemistry, a sulfonate is a salt, anion or ester of a sulfonic acid. Its formula is R−S(=O) 2 −O −, containing the functional group −S(=O) 2 −O −, where R is typically an organyl group, amino group or a halogen atom. Sulfonates are the conjugate bases of sulfonic acids.
These polymers are derived from polystyrene by the addition of sulfonate functional groups. Sodium polystyrene sulfonate was approved for medical use in the United States in 1958. [1] A polystyrene sulfonate was developed in the 2000s to treat Clostridioides difficile associated diarrhea under the name Tolevamer, [2] but it was never marketed.
Although available commercially, the salt can be prepared from sodium dithionite and formaldehyde: . Na 2 S 2 O 4 + 2 CH 2 O + H 2 O → HO-CH 2-SO 3 Na + HO-CH 2-SO 2 Na. This reaction proceeds quantitatively, such that dithionite can be determined by its conversion to Rongalite, which is far less O 2-sensitive and thus easier to handle.
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