Pharmacopoeia and Impurity Reference Standards

Pharmacopoeia and Impurity Reference Standards

Pharmacopoeia and impurity reference standards are authoritative materials used to verify drug identity, purity, potency, and impurity profiles in compliance with USP, EP, JP, ChP, and other global pharmacopeial requirements. These standards include active pharmaceutical ingredient (API) markers, degradation products, synthesis impurities, genotoxic impurities, and system suitability standards. They support method validation, stability studies, impurity qualification, and regulatory submission. Pharmacopoeial standards ensure consistent pharmaceutical quality and patient safety by enabling precise quantification of trace impurities and confirmation of drug specifications. Their certification involves rigorous analytical characterization, inter-laboratory validation, and continuous monitoring of stability.

Benzylpenillic Acid CAS NO 13093-87-3

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CAS No.:13093-87-3

Grade:Pharmacy Grade

Content:99.90%

Packaging:Customizable

Chlorpromazine Ep Impurity F CAS NO 13094-24-1

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CAS No.:13094-24-1

Grade:Pharmacy Grade

Content:99.90%

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Alverine Citrate Impurity C CAS NO 13125-63-8

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CAS No.:13125-63-8

Grade:Pharmacy Grade

Content:99.90%

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Dexamethasone Ep Impurity E CAS NO 13209-41-1

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CAS No.:13209-41-1

Grade:Pharmacy Grade

Content:99.90%

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Fluphenazine Decanoate Impurity 5 CAS NO 13220-06-9

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CAS No.:13220-06-9

Grade:Pharmacy Grade

Content:99.90%

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n-Amyl-n-Methylnitrosamine CAS NO 13256-07-0

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CAS No.:13256-07-0

Grade:Pharmacy Grade

Content:99.90%

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Vinylethylnitrosamine CAS NO 13256-13-8

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CAS No.:13256-13-8

Grade:Pharmacy Grade

Content:99.90%

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Racecadotril Impurity 15 CAS NO 13261-70-6

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CAS No.:13261-70-6

Grade:Pharmacy Grade

Content:99.90%

Packaging:Customizable

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