Gemcitabine Impurity 28 is a fully characterized chemical compound used as a reference standard of API Gemcitabine. The standard offered is compliant with regulatory guidelines. Gemcitabine Impurity 28 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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Gemcitabine EP Impurity A (Cytosine, Lamivudine EP Impurity E)
M.F.
M.W. 111.1
CAT# AR-G01217
CAS# 71-30-7
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Gemcitabine
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Gemcitabine
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Gemcitabine
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Gemcitabine
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Gemcitabine Triphosphate-13C-15N2 Tri(triethylamine) Salt
M.F.
M.W. 506.12 3 101.19
CAT# AR-G01222
CAS# NA
Gemcitabine
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Gemcitabine Diphosphate-13C-15N2 Tri(triethylamine) Salt
M.F.
M.W. 426.14 3 101.19
CAT# AR-G01224
CAS# NA
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alpha-Gemcitabine-13C-15N2 HCl
M.F.
M.W. 266.18 36.46
CAT# AR-G01208
CAS# 122111-05-1 (non-labelled)
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Gemcitabine Triphosphate-13C-15N2 Tri(triethylamine) Salt
M.F.
M.W. 506.12 3 101.19
CAT# AR-G02147
CAS# NA
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Gemcitabine Diphosphate-13C-15N2 Tri(triethylamine) Salt
M.F.
M.W. 426.14 3 101.19
CAT# AR-G02148
CAS# NA
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Gemcitabine EP Impurity B-13C-15N2 (alpha-Gemcitabine-13C-15N2)
M.F.
M.W. 266.18
CAT# AR-G02179
CAS# 1263030-67-6
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