(_D_) _N_/1 _Caustic Soda Free from Carbonate._--Prepared as above and carefully standardized. Some caustic soda solutions show a marked diminution in strength after being boiled; such solutions should be rejected.

(_E_) _N_/1 _Acid._--Carefully standardized.

Soap-Making Manual — Part 101

(_F_) _Phenolphthalein Solution._--0.5 per cent. phenolphthalein in alcohol and neutralized.

Soap-Making Manual — Part 101

In a narrow-mouthed flask (preferably round-bottomed), capacity about 120 cc., which has been thoroughly cleaned and dried, weigh accurately and as rapidly as possible 1.25 to 1.5 grams of the glycerine. A Grethan or Lunge pipette will be found convenient. Add about 3 grams of the anhydrous sodium acetate, then 7.5 cc. of the acetic anhydride, and connect the flask with an upright Liebig condenser. For convenience the inner tube of this condenser should not be over 50 cm. long and 9 to 10 mm. inside diameter. The flask is connected to the condenser by either a ground glass joint (preferably) or a rubber stopper. If a rubber stopper is used it should have had a preliminary treatment with hot acetic anhydride vapor.

Soap-Making Manual — Part 101

Heat the contents and keep just boiling for one hour, taking precautions to prevent the salts drying on the sides of the flask.

Allow the flask to cool somewhat, and through the condenser tube add 50 cc. of distilled water free from carbon dioxide at a temperature of about 80° C., taking care that the flask is not loosened from the condenser. The object of cooling is to avoid any sudden rush of vapors from the flask on adding water, and to avoid breaking the flask. Time is saved by adding the water before the contents of the flask solidify, but the contents may be allowed to solidify and the test proceeded with the next day without detriment, bearing in mind that the anhydride in excess is much more effectively hydrolyzed in hot than in cold water. The contents of the flask may be warmed to, but must not exceed, 80° C., until the solution is complete, except a few dark flocks representing organic impurities in the crude. By giving the flask a rotary motion, solution is more quickly effected.

Cool the flask and contents without loosening from the condenser. When quite cold wash down the inside of the condenser tube, detach the flask, wash off the stopper or ground glass connection into the flask, and filter the contents through an acid-washed filter into a Jena glass flask of about 1 litre capacity. Wash thoroughly with cold distilled water free from carbon dioxide. Add 2 cc. of phenolphthalein solution (_F_), then run in caustic soda solution (_C_) or (_D_) until a faint pinkish yellow color appears throughout the solution. This neutralization must be done most carefully; the alkali should be run down the sides of the flask, the contents of which are kept rapidly swirling with occasional agitation or change of motion until the solution is nearly neutralized, as indicated by the slower disappearance of the color developed locally by the alkali running into the mixture. When this point is reached the sides of the flask are washed down with carbon dioxide-free water and the alkali subsequently added drop by drop, mixing after each drop until the desired tint is obtained.