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Saponification is a process of cleaving esters into carboxylate salts and alcohols by the action of aqueous alkali. Typically aqueous sodium hydroxide solutions are used. [1] [2] It is an important type of alkaline hydrolysis. When the carboxylate is long chain, its salt is called a soap. The saponification of ethyl acetate gives sodium acetate ...
In a typical preparation, 255 mL of a solution with 118 g/L HClO is slowly added with stirring to a solution of 40 g of NaOH in water 0 °C. Some sodium chloride precipitates and is removed by filtration. The solution is vacuum evaporated at 40–50 °C and 1–2 mmHg until the dihydrate crystallizes out. The crystals are vacuum-dried to ...
Example of saponification reaction of a triglyceride molecule (left) with potassium hydroxide (KOH) yielding glycerol (purple) and salts of fatty acids ().. Saponification value or saponification number (SV or SN) represents the number of milligrams of potassium hydroxide (KOH) or sodium hydroxide (NaOH) required to saponify one gram of fat under the conditions specified.
Sodium dodecyl sulfate (SDS) or sodium lauryl sulfate (SLS), sometimes written sodium laurilsulfate, is an organic compound with the formula CH 3 (CH 2) 11 OSO 3 Na and structure H 3 C−(CH 2) 11 −O−S(=O) 2 −O − Na +. It is an anionic surfactant used in many cleaning and hygiene products. This compound is the sodium salt of the 12 ...
It is a sodium salt of the orthoboric acid B(OH) 3. The compound is also called trisodium orthoborate, sodium orthoborate, or just sodium borate. However, "sodium orthoborate" has been used also for a compound with formula Na 4 B 2 O 5, which would correspond to an equimolar mixture of sodium metaborate NaBO 2 and trisodium borate proper.
3, which is the main component of commercial sodium silicate solutions. It is an ionic compound consisting of sodium cations Na + and the polymeric metasilicate anions [– SiO 2− 3 –] n. It is a colorless crystalline hygroscopic and deliquescent solid, soluble in water (giving an alkaline solution) but not in alcohols. [1]
This process, called saponification, breaks down the triglyceride (fat); frees the glycerol within; and, results in a sodium salt, sodium tallowate. It is usually combined with sodium cocoate, the sodium salt of coconut oil. Together, they are—with sodium palmate—major constituents of bar soap.
In this reaction, the triglyceride fats are first hydrolyzed into free fatty acids, and then these combine with the alkali to form crude soap: a combination of various soap salts, excess fat or alkali, water, and liberated glycerol (glycerin). [9] Saltwater soaps are potassium salts rather than sodium salts. Both sodium and potassium are alkali ...