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Pharmaceutical analytical standards

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

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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

ZZR Impurity 165

ImpurityLevels of characterisation

Cat. No.: P-Z066-167
Formula: C₂₃H₃₈N₂OS₂

ZZR Impurity 17

ImpurityLevels of characterisation

Cat. No.: P-Z066-019
Formula: C₂₀H₂₈FN₃OS

ZZR Impurity 18

ImpurityLevels of characterisation

Cat. No.: P-Z066-020
Formula: C₂₁H₂₉FN₂OS₂

ZZR Impurity 19

ImpurityLevels of characterisation

Cat. No.: P-Z066-021
Formula: C₂₁H₃₀FN₃OS

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