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Pharmaceutical analytical standards

Active ingredients, pharmacopoeial impurities, metabolites, nitrosamines and labelled standards.

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ZZR Impurity 156

ImpurityLevels of characterisation

Cat. No.: P-Z066-158
Formula: C₂₁H₃₃F₂N₃OS

ZZR Impurity 157

ImpurityLevels of characterisation

Cat. No.: P-Z066-159
Formula: C₂₁H₃₂F₂N₂OS₂

ZZR Impurity 158

ImpurityLevels of characterisation

Cat. No.: P-Z066-160
Formula: C₂₁H₃₃F₂N₃OS

ZZR Impurity 159

ImpurityLevels of characterisation

Cat. No.: P-Z066-161
Formula: C₂₁H₃₂F₂N₂OS₂

ZZR Impurity 16

ImpurityLevels of characterisation

Cat. No.: P-Z066-018
Formula: C₂₁H₃₁N₃OS

ZZR Impurity 160

ImpurityLevels of characterisation

Cat. No.: P-Z066-162
Formula: C₂₃H₃₉N₃OS

ZZR Impurity 161

ImpurityLevels of characterisation

Cat. No.: P-Z066-163
Formula: C₂₃H₃₈N₂OS₂

ZZR Impurity 162

ImpurityLevels of characterisation

Cat. No.: P-Z066-164
Formula: C₂₃H₃₉N₃OS

ZZR Impurity 163

ImpurityLevels of characterisation

Cat. No.: P-Z066-165
Formula: C₂₃H₃₈N₂OS₂

ZZR Impurity 164

ImpurityLevels of characterisation

Cat. No.: P-Z066-166
Formula: C₂₃H₃₉N₃OS

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