2-(2-aminobut-3-en-1-yl)malonic acid
Vigabatrin EP Impurity E is a fully characterized chemical compound used as a reference standard of API Vigabatrin. The standard offered is compliant with regulatory guidelines. Vigabatrin EP Impurity E 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 - 1378466-25-1
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Vigabatrin
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Vigabatrin EP Impurity B HCl (Mixture of Z and E Isomers)

M.F. C₆H₁₁NO₂. HCl
M.W. 129.16 36.46
CAT# AR-V01343
CAS# NA
Vigabatrin
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Vigabatrin
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4-oxo-6-(2-oxo-5-vinylpyrrolidin-1-yl)hexanoic acid

M.F. C₁₂H₁₇NO₄
M.W. 239.27
CAT# AR-V01349
CAS# NA
Vigabatrin
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Vigabatrin EP Impurity C (Mixture of Diastereomers)

M.F. C₇H₁₀N₂O₂
M.W. 154.17
CAT# AR-V01344
CAS# 71107-19-2
Vigabatrin
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Vigabatrin EP Impurity F HCl (Mixture of Diastereomers)

M.F. C₁₂H₂₀N₂O₃. HCl
M.W. 240.30 36.46
CAT# AR-V01347
CAS# 794466-81-2 (free base)
Vigabatrin
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Vigabatrin
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Vigabatrin
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Vigabatrin
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Vigabatrin
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Vigabatrin-13C-d2 HCl

M.F. ₁₃C C₅H₉D₂NO₂. HCl
M.W. 132.16 36.46
CAT# AR-V01341
CAS# 1391054-02-6 (non-labelled)
Vigabatrin
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