Serine
Click to View Image
C3H7NO3 105.09

l-Serine
l-Serine [56-45-1].
» Serine contains not less than 98.5 percent and not more than 101.5 percent of C3H7NO3, as l-serine, calculated on the dried basis.
Packaging and storage— Preserve in well-closed containers.
Identification, Infrared Absorption 197K.
Specific rotation 781S: between +14.0 and +15.6.
Test solution: 100 mg per mL, in 2 N hydrochloric acid.
Loss on drying 731 Dry it at 105 for 3 hours: it loses not more than 0.2% of its weight.
Residue on ignition 281: not more than 0.1%.
Chloride 221 A 0.73-g portion shows no more chloride than corresponds to 0.50 mL of 0.020 N hydrochloric acid (0.05%).
Sulfate 221 A 0.33-g portion shows no more sulfate than corresponds to 0.10 mL of 0.020 N sulfuric acid (0.03%).
Iron 241: 0.003%.
Chromatographic purity—
Adsorbent: 0.25-mm layer of chromatographic silica gel mixture.
Test solution— Dissolve an accurately weighed quantity of Serine in 0.1 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-Serine RS in 0.1 N hydrochloric acid to obtain a solution having a known concentration of about 0.05 mg per mL. Apply 5 µL. [note—This solution has a concentration equivalent to about 0.5% of that of the Test solution.]
System suitability solution— Prepare a solution in 0.1 N hydrochloric acid containing 0.4 mg each of USP L-Serine RS and USP L-Methionine 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 621. After air-drying the plate, spray with Spray reagent, and heat between 100 and 105 for about 15 minutes. Examine the plate under white light. The chromatogram obtained from the System suitability solution exhibits two clearly separated spots. Any secondary spot in the chromatogram obtained from the Test solution is not larger or more intense than the principal spot in the chromatogram obtained from the Standard solution: not more than 0.5% of any individual impurity is found; and not more than 2.0% of total impurities is found.
Assay— Transfer about 100 mg of Serine, 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 10.51 mg of C3H7NO3.
Auxiliary Information— Please check for your question in the FAQs before contacting USP.
Topic/Question Contact Expert Committee
Monograph Curtis Phinney

1-301-816-8540
(DSN05) Dietary Supplements - Non-Botanicals
Reference Standards Lili Wang, Technical Services Scientist
1-301-816-8129
RSTech@usp.org
USP32–NF27 Page 3551
Chromatographic Column—
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.