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Diethylsuccinoylsuccinate is an organic compound with the formula [CH 2 C(OH)=C(CO 2 Et)] 2 (Et = ethyl). A tetrasubstituted derivative of 1,4-cyclohexadiene, the compound is the enol tautomer of the corresponding cyclohexadione. [1] It is produced by base-induced condensation of diethyl succinate: [2] 2 EtO 2 CCH 2 CH 2 CO 2 Et [CH 2 C(OH)=C ...
Diethyl succinate is the diethyl ester of succinate. It is a colorless liquid with the formula (CH 2 CO 2 Et) 2 (Et = ethyl). The organic molecule contains two ester groups. This ester is a versatile chemical intermediate. A colorless liquid, diethyl succinate is formed by Fischer esterification of succinic acid and ethanol.
Dioctyl sebacate (also di(2-ethylhexyl) sebacate, commonly abbreviated as DOS, DEHS, and BEHS) is an organic compound which is the diester of sebacic acid and 2-ethylhexanol. It is an oily colorless liquid and is used as a plasticizer , including in the explosive C4 . [ 1 ]
Bis(2-ethylhexyl) adipate or DEHA or DOA is an organic compound with the formula (CH 2 CH 2 CO 2 C 8 H 17) 2. It is the diester of 2-ethylhexanol and adipic acid. It is a colorless oily liquid. DEHA is sometimes called "dioctyl adipate", incorrectly. Another name is di(2-ethylhexyl) adipate.
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.
The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
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 ]
Bis(2-ethylhexyl) maleate is the chemical compound with the structural formula (H 3 C(−CH 2) 3 −CH(−CH 2 −CH 3)−CH 2 −O−C(=O)−CH=) 2, where the two carboxylate groups are mutually cis. It can be described as the double ester of maleic acid with the alcohol 2-ethylhexanol.