Formoterol Impurity 10 is a fully characterized chemical compound used as a reference standard of API Lumacaftor. The standard offered is compliant with regulatory guidelines. Formoterol Impurity 10 is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - NA
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Formoterol EP Impurity E (Mixture of Diastereomers)
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M.W. 434.54
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Formoterol EP Impurity D Fumarate (Mixture of Diastereomers)
M.F. C₂₀H₂₆N₂O₄ C₄H₄O₄
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Formoterol Fumarate Dihydrate
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M.W. 2(344.40);116.07;2(18.02)
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Formoterol EP Impurity A (Mixture of Diastereomers)
M.F. C₁₈H₂₄N₂O₃
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M.F. C₁₈H₂₁N₂O₄ ₁₃CD₃. ₀.₅C₄H₄O₄
M.W. 348.42 0.5 116.07
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