Clarithromycin Impurity 17 is a fully characterized chemical compound used as a reference standard of API Clarithromycin. The standard offered is compliant with regulatory guidelines. Clarithromycin Impurity 17 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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Clarithromycin EP Impurity D (N-Desmethyl Clarithromycin)
M.F.
M.W. 733.94
CAT# AR-C03024
CAS# 101666-68-6
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Clarithromycin USP Impurity Q (Clarithromycin N-Oxide)
M.F.
M.W. 763.96
CAT# AR-C03026
CAS# 118074-07-0
Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin EP Impurity G (Mixture of Z and E Isomers)
M.F.
M.W. 777.01
CAT# AR-E00998
CAS# 107216-09-1
Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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N-(3-Desethynylphenyl)-N-(3-bromophenyl) Erlotinib Hydrochloride
M.F.
M.W. 448.31 36.5
CAT# AR-E02315
CAS# 2055840-41-8
Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin Impurity 3 (6-O-methylerythronolide A)
M.F.
M.W. 432.55
CAT# AR-C07824
CAS# 2376120-29-3
Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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Clarithromycin
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