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Threonine
» Threonine contains not less than 98.5 percent and not more than 101.5 percent of C4H9NO3, as l-threonine, calculated on the dried basis.
Packaging and storage
Preserve in well-closed containers.
pH
Loss on drying
Residue on ignition
Chloride
Sulfate
Iron
Heavy metals, Method I
Chromatographic purity
Adsorbent:
0.25-mm layer of chromatographic silica gel mixture.
Diluent
Prepare by mixing 10 mL of hydrochloric acid with sufficient water to make 1000 mL.
Test solution
Dissolve an accurately weighed quantity of Threonine in 2 N hydrochloric acid to obtain a solution having a concentration of 10 mg per mL. Apply 5 µL.
Standard solution
Dissolve an accurately weighed quantity of USP l-Threonine RS in Diluent to obtain a solution having a known concentration of about 0.05 mg per mL. Apply 5 µL. [noteThis solution has a concentration equivalent to about 0.5% of that of the Test solution.]
System suitability solution
Prepare a solution in Diluent containing 0.4 mg each of USP l-Threonine RS and USP l-Proline RS per mL. Apply 5 µL.
Spray reagent
Dissolve 0.2 g of ninhydrin in 100 mL of a mixture of butyl alcohol and 2 N acetic acid (95:5).
Developing solvent system
Prepare a mixture of butyl alcohol, glacial acetic acid, and water (60:20:20).
Procedure
Proceed as directed for Thin-Layer Chromatography under Chromatography
Assay
Transfer about 110 mg of Threonine, accurately weighed, to a 125-mL flask, dissolve in a mixture of 3 mL of formic acid and 50 mL of glacial acetic acid, and titrate with 0.1 N perchloric acid VS, determining the endpoint potentiometrically. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N perchloric acid is equivalent to 11.91 mg of C4H9NO3.
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
Chromatographic Column
USP32NF27 Page 3735
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
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