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In a classic laboratory procedure, the triglyceride trimyristin is obtained by extracting it from nutmeg with diethyl ether. Saponification to the soap sodium myristate takes place using NaOH in water. Treating the soap with hydrochloric acid gives myristic acid. [4]
Bottle of 20% sodium dodecyl sulfate in distilled water for use in the laboratory. The critical micelle concentration (CMC) in water at 25 °C is 8.2 mM, [1] and the aggregation number at this concentration is usually considered to be about 62. [3] The micelle ionization fraction (α) is around 0.3 (or 30%). [4]
A handmade soap bar Two equivalent images of the chemical structure of sodium stearate, a typical ingredient found in bar soaps Emulsifying action of soap on oil. Soap is a salt of a fatty acid (sometimes other carboxylic acids) used for cleaning and lubricating products as well as other applications. [1]
During the Nuremberg trials, Sigmund Mazur, a laboratory assistant at the Danzig Anatomical Institute, testified that soap had been made from corpse fat at the institute, and he also claimed that 70 to 80 kg (155–175 lb) of fat which was collected from 40 bodies could produce more than 25 kg (55 lb) of soap, and the finished soap was retained ...
Linear alkylbenzenes (sometimes also known as LABs) are a family of organic compounds with the formula C 6 H 5 C n H 2n+1. Typically, n lies between 10 and 16, although generally supplied as a tighter cut, such as C 12 -C 15 , C 12 -C 13 and C 10 -C 13 , for detergent use. [ 1 ]
Glycerin soap can also be produced without remelting soap through directly cooking raw home-made soap. [3] Modern clear glycerin soaps bases are produced by combining various glycerol and polyols with soap and other surfactants in a manner similar to traditional glycerin soap-making methods. These modern clear soaps have the benefit of being ...