Gadobutrol Impurity 10 is a fully characterized chemical compound used as a reference standard of API Gadoteridol. The standard offered is compliant with regulatory guidelines. Gadobutrol 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 -
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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1,4,7,10-tetrabenzyl-1,4,7,10-tetraazacyclododecane

M.F. C₃₆H₄₄N₄
M.W. 532.78
CAT# AR-G01034
CAS# 18084-64-5
Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadoteridol
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Gadobutrol Impurity 1 (mix of enantiomers)

M.F. C₁₈H₃₄N₄O₉
M.W. 450.49
CAT# AR-G01030
CAS# 138168-36-2 (racemic mix)
Gadoteridol
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Gadobutrol EP Impurity C (Gd-DO3A)

M.F. C₁₄H₂₃N₄O₆. Gd
M.W. 343.36 157.25
CAT# AR-G01032
CAS# 112188-16-6
Gadoteridol
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Gadobutrol Impurity 2 4HCl (Mixture of Diastereomers)

M.F. C₂₀H₄₀N₄O₁₀. ₄ HCl
M.W. 496.56 4 36.46
CAT# AR-G01031
CAS# 2514736-59-3
Gadoteridol
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