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Docusate is the common chemical and pharmaceutical name of the anion bis(2-ethylhexyl) sulfosuccinate, also commonly called dioctyl sulfosuccinate (DOSS). [ 2 ] [ 3 ] [ 4 ] Salts of this anion, especially docusate sodium , are widely used in medicine as an emollient laxative and as stool softeners , by mouth or rectally. [ 1 ]
It is a key intermediate raw material in the production of dioctyl sulfosuccinate (DOSS, docusate) salts, used medically as laxatives and stool softeners, and in many other applications as versatile surfactants. [2] [3] [4]
Structure of sodium sulfosuccinate esters. Sodium sulfosuccinate esters are organic compounds with the formula NaO 3 SCH(CO 2 R')CH 2 CO 2 R where R and R' can be H or alkyl groups. They comprise a large class of surfactants and emulsifiers used in cosmetics, pharmaceuticals, and cleaning agents. They are colorless salts.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
I oppose. We do not need seperate articles on each salt. Docusate is also the common name. Doc James (talk · contribs · email) 21:58, 12 November 2018 (UTC) @Doc James: While "docusate" is the material's WP:COMMONNAME it appears that "docusate sodium" is how the stool softener product is labeled. Do a Google image search for "docusate salt".
Bis(2-ethylhexyl) phthalate (di-2-ethylhexyl phthalate, diethylhexyl phthalate, diisooctyl phthalate, DEHP; incorrectly — dioctyl phthalate, DIOP) is an organic compound with the formula C 6 H 4 (CO 2 C 8 H 17) 2. DEHP is the most common member of the class of phthalates, which are used as plasticizers.
Sodium methylsulfinylmethylide (also called NaDMSO or dimsyl sodium) is the sodium salt of the conjugate base of dimethyl sulfoxide. This unusual salt has some uses in organic chemistry as a base and nucleophile. Since the first publication in 1965 by Corey et al., [2] a number of additional uses for this reagent have been identified. [3]
Sodium polysulfide can be produced by dissolving sulfur in a solution of sodium sulfide. [4] Alternatively they are produced by the redox reaction of aqueous sodium hydroxide with sulfur at elevated temperatures. [5] Finally they arise by the reduction of elemental sulfur with sodium, a reaction often conducted in anhydrous ammonia.