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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 ...
Halazone's disinfecting activity is mainly due to the hypochlorous acid (HClO) released by hydrolysis of the chlorine-nitrogen bonds when the product is dissolved in water: [8] (R1)(R2)NCl + H 2 O → HOCl + (R1)(R2)NH. The hypochlorous acid is a powerful oxidizer and chlorinating agent that destroys or denatures many organic compounds.
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.
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]
A diuretic tablet is sometimes colloquially called a water tablet. There are several categories of diuretics. There are several categories of diuretics. All diuretics increase the excretion of water from the body, through the kidneys .
Denatonium, usually available as denatonium benzoate (under trade names such as Denatrol, BITTERANT-b, BITTER+PLUS, Bitrex, Bitrix, and Aversion) and as denatonium saccharinate (BITTERANT-s), is the most bitter chemical compound known, with bitterness thresholds of 0.05 ppm for the benzoate and 0.01 ppm for the saccharinate. [1]
Malathion is an acetylcholinesterase inhibitor, a diverse family of chemicals.Upon uptake into the target organism, it binds irreversibly to the serine residue in the active catalytic site of the cholinesterase enzyme.
After tablets came "computer acid" or "blotter paper LSD," typically made by dipping a preprinted sheet of blotting paper into an LSD/water/alcohol solution. [ 208 ] [ 209 ] More than 200 types of LSD tablets have been encountered since 1969 and more than 350 blotter paper designs have been observed since 1975. [ 209 ]