Tartaric Acid
Click to View Image
C4H6O6 150.09

Butanedioic acid, 2,3-dihydroxy-; Butanedioic acid, 2,3-dihydroxy-, [R-(R*,R*)]-.
Tartaric acid; l -(+)-Tartaric acid [526-83-0] and [87-69-4].
» Tartaric Acid, dried over phosphorus pentoxide for 3 hours, contains not less than 99.7 percent and not more than 100.5 percent of C4H6O6.
Packaging and storage— Preserve in well-closed containers.
Identification—
A: It responds to the tests for Tartrate 191.
B: When ignited, it gradually decomposes, emitting an odor resembling that of burning sugar (distinction from citric acid).
Specific rotation 781S: between +12.0 and +13.0.
Test solution: 200 mg per mL, in water.
Loss on drying 731 Dry it over phosphorus pentoxide for 3 hours: it loses not more than 0.5% of its weight.
Residue on ignition 281: not more than 0.1%.
Limit of oxalate— Nearly neutralize 10 mL of a solution of it (1 in 10) with 6 N ammonium hydroxide, and add 10 mL of calcium sulfate TS: no turbidity is produced.
Sulfate 221 To 10 mL of a solution (1 in 100) add 3 drops of hydrochloric acid and 1 mL of barium chloride TS: no turbidity is produced.
Assay— Place about 2 g of Tartaric Acid, previously dried and accurately weighed, in a conical flask. Dissolve it in 40 mL of water, add phenolphthalein TS, and titrate with 1 N sodium hydroxide VS. Each mL of 1 N sodium hydroxide is equivalent to 75.04 mg of C4H6O6.
Auxiliary Information— Please check for your question in the FAQs before contacting USP.
Topic/Question Contact Expert Committee
Monograph Robert H. Lafaver, B.A.
Scientist
1-301-816-8335
(EM105) Excipient Monographs 1
USP32–NF27 Page 1368
Chromatographic Column—
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.