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    Albuterol

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    Albuterol

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    Albuterol

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    Printed on: Wed Feb 08 2023, 11:21:25 PM(EST) Status: Currently Official on 09-Feb-2023 DocId: GUID-1F1BDF7C-D2BA-4B37-AB82-54839066E0F5_3_en-US

    Printed by: Dang Van Vu Official Date: Official as of 01-May-2020 Document Type: USP @2023 USPC
    Do Not Distribute DOI Ref: u8l5c DOI: https://doi.org/10.31003/USPNF_M1195_03_01
    1

    IMPURITIES
    Albuterol • RESIDUE ON IGNITION á281ñ: NMT 0.1%
    • ORGANIC IMPURITIES
    Standard solution: 0.10 mg/mL of USP Albuterol RS in
    methanol
    Sample solution: 20 mg/mL of Albuterol in methanol
    Chromatographic system
    C13H21NO3 239.31 (See Chromatography á621ñ, Thin-Layer Chromatography.)
    1,3-Benzenedimethanol, α1-[[(1,1-dimethylethyl)amino] Mode: TLC
    methyl]-4-hydroxy-; Adsorbent: 0.25-mm layer of chromatographic silica gel
    α1-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,α′-diol Application volume: 10 µL
    CAS RN®: 18559-94-9; UNII: QF8SVZ843E. Developing solvent system: Methyl isobutyl ketone,
    DEFINITION isopropyl alcohol, ethyl acetate, ammonium hydroxide,
    Albuterol contains NLT 98.5% and NMT 101.0% of albuterol and water (50:45:35:3:18)
    (C13H21NO3), calculated on the anhydrous basis. Visualization: Iodine vapor
    Analysis
    IDENTIFICATION Samples: Standard solution and Sample solution
    Proceed as directed in the chapter, applying aliquots of
    Change to read: the Standard solution and the Sample solution. Develop
    • A. ▲SPECTROSCOPIC IDENTIFICATION TESTS á197ñ, Infrared in the Developing solvent system until the solvent front
    Spectroscopy: 197K▲ (CN 1-May-2020) has moved three-fourths the length of the plate. Remove
    the plate from the developing chamber, air-dry, and

    al
    expose it to iodine vapor.
    Change to read: Acceptance criteria: Any spot, other than the principal
    • B. ▲SPECTROSCOPIC IDENTIFICATION TESTS á197ñ, spot, obtained from the Sample solution is not greater in size
    Ultraviolet-Visible Spectroscopy: 197U▲ (CN 1-May-2020) and intensity than the spot produced by the Standard
    Sample solution: 80 µg/mL in 0.1 N hydrochloric acid solution (0.5%), and the sum of the impurities is not greater
    than 2.0%.
    Acceptance criteria: Meets the requirements
    ASSAY
    • PROCEDURE
    ci SPECIFIC TESTS
    • WATER DETERMINATION, Method I á921ñ: NMT 0.5%
    Sample solution: 8 mg/mL of Albuterol in glacial acetic acid ADDITIONAL REQUIREMENTS
    Analysis: To 50 mL of the Sample solution add 2 drops of • PACKAGING AND STORAGE: Preserve in well-closed,
    ffi
    crystal violet TS, and titrate with 0.1 N perchloric acid VS. light-resistant containers.
    Perform a blank determination, and make any necessary • USP REFERENCE STANDARDS á11ñ
    correction. Each mL of 0.1 N perchloric acid is equivalent USP Albuterol RS
    to 23.93 mg of C13H21NO3.
    Acceptance criteria: 98.5%–101.0% on the anhydrous
    basis
    O

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