Mesalazine Impurity 12 is a fully characterized chemical compound used as a reference standard of API Mesalamine. The standard offered is compliant with regulatory guidelines. Mesalazine Impurity 12 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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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalazine (Mesalamine) EP Impurity G Ethanolamine
M.F.
M.W. 154.12 61.08
CAT# AR-M04243
CAS# 7491-35-2
Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine Impurity 8 HCl (5-Hydroxyanthranilic Acid HCl)
M.F.
M.W. 153.14 36.46
CAT# AR-M04256
CAS# 2133-03-1
Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalazine (Mesalamine) EP Impurity A-d4 (Paracetamol EP Impurity K-d4)
M.F.
M.W. 113.15
CAT# AR-M04233
CAS# NA
Mesalamine
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Mesalamine
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Mesalamine
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Mesalamine
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Mesalazine (Mesalamine) EP Impurity L-d4 (Mefenamic Acid EP Impurity C-d4)
M.F.
M.W. 160.59
CAT# AR-M04258
CAS# 1219795-28-4
Mesalamine
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