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Abacavir EP Impurity F

N° de SZ CAT:SZ-A049007
Número CAS1443421-68-8
Mol.F.C18H26N6O
Peso Molecular342.4
Status de FaturaUnder Synthesis

Nome Químico: 6-(Cyclopropylamino)-9-[(1R,4S)-4-[[(1,1-dimethylethyl)oxy]methyl]cyclopent-2-enyl]-9H-purine-2-amine (as per EP) ; 9-[(1R,4S)-4-(tert-Butoxymethyl)cyclopent-2-enyl]-N6-cyclopropyl-9H-purine-2,6-diamine (as per USP)

Sinônimo: O-t-Butyl Derivative Abacavir (USP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: [H][C@@]1(C=C[C@](COC(C)(C)C)([H])C1)N2C3=NC(N)=NC(NC4CC4)=C3N=C2

Abacavir EP Impurity F is chemically 6-(Cyclopropylamino)-9-[(1R,4S)-4-[[(1,1-dimethylethyl)oxy]methyl]cyclopent-2-enyl]-9H-purine-2-amine (as per EP) ; 9-[(1R,4S)-4-(tert-Butoxymethyl)cyclopent-2-enyl]-N6-cyclopropyl-9H-purine-2,6-diamine (as per USP). It is also known as O-t-Butyl Derivative Abacavir (USP). Abacavir EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Abacavir EP Impurity F can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Abacavir.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

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