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Pharmaceutical analytical standards

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

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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

ZZR Impurity 2

ImpurityLevels of characterisation

Cat. No.: P-Z066-004
Formula: C₂₁H₃₀N₂O₂

ZZR Impurity 20

ImpurityLevels of characterisation

Cat. No.: P-Z066-022
Formula: C₁₉H₂₈N₄OS

ZZR Impurity 21

ImpurityLevels of characterisation

Cat. No.: P-Z066-023
Formula: C₁₈H₂₇N₅OS

ZZR Impurity 22

ImpurityLevels of characterisation

Cat. No.: P-Z066-024
Formula: C₂₀H₂₉N₃OS

ZZR Impurity 23

ImpurityLevels of characterisation

Cat. No.: P-Z066-025
Formula: C₁₉H₂₆ClN₃OS

ZZR Impurity 24

ImpurityLevels of characterisation

Cat. No.: P-Z066-026
Formula: C₂₀H₂₇FN₂OS₂

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