» Calcium Undecylenate contains not less than 98.0 percent and not more than 102.0 percent of C22H38O4Ca (calcium undecylenate), calculated on the dried basis.
Packaging and storage Preserve in well-closed containers.
A: A filtered solution (1 in 20) in 3 N hydrochloric acid responds to the tests for Calcium 191.
B: Transfer 40 mL of water and 10 g of calcium undecylenate to a 250-mL separator. Cautiously and slowly add 10 mL of hydrochloric acid, while swirling. Insert the stopper, and shake. [noteThe separator will become quite warm, and pressure must be carefully and frequently relieved through the stopcock. If a curdy, white material remains after 5 minutes of shaking, add additional hydrochloric acid, 1 mL at a time, and shake until a clear oily phase is formed.] Allow the phases to separate, drain, and discard the bottom aqueous layer. Drain and discard the middle oily layer, if present. Filter the top layer of undecylenic acid through a pledget of cotton into a 10-mL graduated cylinder, noting the volume obtained. Transfer the filtrate to a 250-mL flask, and add an equal volume of aniline. Reflux for 1 hour, swirling the flask occasionally. Allow to cool, and pour 60 mL of alcohol through the condenser into the flask. Remove the flask from the condenser, add 1 g of charcoal, and stir. Filter the slurry into a 250-mL beaker. Add water dropwise until a few crystals form or the solution becomes slightly cloudy. [noteIf too much water is added, an oil will form. Add alcohol dropwise until the oil dissolves.] Allow the mixture to stand or refrigerate until crystals are formed. Collect the crystals on a filter paper inserted in a 45-mm porous glass filter funnel. Wash the crystals with 75 mL of 25% alcohol: the crystals have a clean, white, glossy appearance. If not, recrystallize by dissolving the crystals in about 50 mL of alcohol. Add about 1 g of charcoal, stir, filter into a 150-mL beaker, and continue as directed above, beginning with Add water dropwise. Dry the crystals in vacuum at 50 for 2 hours: the crystals so obtained melt between 66 and 67.5, the procedure for Class Ia being used (see Melting Range or Temperature 741). [noteIf the melting point is low, additional drying or recrystallization may be necessary.]
Loss on drying 731 Dry it at 105 for 2 hours: it loses between 2.0% and 5.7% of its weight.
Particle size, Method I 786 Test in accordance with this procedure, except to use not more than 25 g, and except that a single No. 100 sieve is used and is to be shaken for not less than 30 minutes or until sifting is practically complete: not less than 99.0% of it passes through a No. 100 sieve.
Limit of free undecylenic acid Transfer 10 g of Calcium Undecylenate, accurately weighed, to a 400-mL beaker, add 250 mL of solvent hexane, and mix for 2 hours using a magnetic stirrer. Filter into a 500-mL flask, evaporate with the aid of a current of air to about 20 mL, and add 100 mL of neutralized alcohol. Add 3 drops of phenolphthalein TS, and titrate with 0.1 N sodium hydroxide VS. Each mL of 0.1 N sodium hydroxide is equivalent to 18.43 mg of C11H20O2: not more than 0.1% is found.
Assay Boil 40.0 mL of 0.1 N hydrochloric acid VS with about 600 mg of Calcium Undecylenate, accurately weighed, for 10 minutes, or until the undecylenic acid layer is clear, adding water, as necessary, to maintain the original volume. Transfer the mixture, with the aid of water, to a 500-mL separator. Dilute with water to about 75 mL, and extract with two 100-mL portions of solvent hexane. Wash the combined extracts with water until the last washing is neutral to litmus, add the washings to the original water layer. Cool, add 3 drops of methyl orange TS, and titrate the excess hydrochloric acid with 0.1 N sodium hydroxide VS. Perform a blank determination (see Residual Titrations under Titrimetry 541). Each mL of 0.1 N sodium hydroxide is equivalent to 20.33 mg of C22H38O4Ca.