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Tyrosine
(tye' roe seen).
DEFINITION
Tyrosine contains NLT 98.5% and NMT 101.5% of l-tyrosine (C9H11NO3), calculated on the dried basis.
IDENTIFICATION
ASSAY
• Procedure
Sample:
180 mg of Tyrosine
Blank:
Mix 6 mL of formic acid and 50 mL of glacial acetic acid.
Titrimetric system
(See Titrimetry
Mode:
Direct titration
Titrant:
0.1 N perchloric acid VS
Endpoint detection:
Potentiometric
Analysis:
Dissolve the Sample in 6 mL of formic acid and 50 mL of glacial acetic acid, and titrate with the Titrant. Perform the Blank determination.
Calculate the percentage of tyrosine (C9H11NO3) in the Sample taken:
Result = {[(VS
Acceptance criteria:
98.5%101.5% on the dried basis
IMPURITIES
• Residue on Ignition
• Chloride and Sulfate, Chloride
Standard solution:
0.20 mL of 0.020 N hydrochloric acid
Sample:
0.35 g of Tyrosine. [NoteIf necessary, dissolve the Sample by heating to near boiling and adding 1 mL of nitric acid. ]
Acceptance criteria:
NMT 0.04%
• Chloride and Sulfate, Sulfate
Standard solution:
0.50 mL of 0.020 N sulfuric acid
Sample:
1.2 g of Tyrosine. [NoteIf necessary, dissolve the Sample by adding 6 mL of diluted hydrochloric acid. ]
Acceptance criteria:
NMT 0.04%
• Iron
• Heavy Metals, Method I
• Related Compounds
Diluted ammonia solution:
Dilute 16 mL of concentrated ammonia with water to 100 mL.
System suitability solution:
Dissolve 10 mg of USP l-Tyrosine RS and 10 mg of USP l-Phenylalanine RS in 1 mL of Diluted ammonia solution, and dilute with water to 25.0 mL.
Standard solution:
In a suitable flask, dissolve a quantity of USP l-Tyrosine RS in 1 mL of Diluted ammonia solution. Dilute with water to volume to obtain a solution of 0.05 mg/mL. [NoteThis solution has a concentration equivalent to 0.5% of that of the Sample solution. ]
Sample solution:
Transfer 0.1 g of Tyrosine into a 10-mL volumetric flask, add sufficient Diluted ammonia solution to dissolve, and dilute with water to volume.
Chromatographic system
Mode:
TLC
Adsorbent:
0.25-mm layer of chromatographic silica gel mixture
Application volume:
5 µL
Developing solvent system:
Isopropyl alcohol and ammonium hydroxide (7:3)
Spray reagent:
2 mg/mL of ninhydrin in a mixture of butyl alcohol and 2 N acetic acid (95:5)
System suitability
Suitability requirements:
The chromatogram of the System suitability solution exhibits two clearly separated spots.
Analysis
Samples:
System suitability solution, Standard solution, and Sample solution
Dry the plate between 100
Acceptance criteria:
Any secondary spot of the Sample solution is not larger or more intense than the principal spot of the Standard solution.
Any individual impurity:
NMT 0.5%
Total impurities:
NMT 2.0%
SPECIFIC TESTS
• Optical Rotation, Specific Rotation
Sample solution:
50 mg/mL in 1 N hydrochloric acid
Acceptance criteria:
• Loss on Drying
ADDITIONAL REQUIREMENTS
• Packaging and Storage:
Preserve in well-closed containers.
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP35NF30 Page 4976
Pharmacopeial Forum: Volume No. 32(6) Page 1761
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