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Pharmaceutical analytical standards

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

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ZZR Impurity 150

ImpurityLevels of characterisation

Cat. No.: P-Z066-152
Formula: C₂₁H₃₂Cl₂N₂OS₂

ZZR Impurity 151

ImpurityLevels of characterisation

Cat. No.: P-Z066-153
Formula: C₂₁H₃₃F₂N₃OS

ZZR Impurity 152

ImpurityLevels of characterisation

Cat. No.: P-Z066-154
Formula: C₂₁H₃₂F₂N₂OS₂

ZZR Impurity 153

ImpurityLevels of characterisation

Cat. No.: P-Z066-155
Formula: C₂₁H₃₃F₂N₃OS

ZZR Impurity 154

ImpurityLevels of characterisation

Cat. No.: P-Z066-156
Formula: C₂₁H₃₂F₂N₂OS₂

ZZR Impurity 155

ImpurityLevels of characterisation

Cat. No.: P-Z066-157
Formula: C₂₀H₂₈N₂O₂S
Synonyms: S-Methyl N-[(2-heptyl-3-methyl-4-oxoquinolin-1-yl)methyl]carbamothioate

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

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