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Levothyroxine EP Impurity A

N° de SZ CAT:SZ-L022002
Número CAS55-06-1
Mol.F.C15H11I3NO4 : Na
Peso Molecular650.0 : 23.0
Status de FaturaIn Stock
Rel. CAS No6893-02-3 (free base)

Nome Químico: Sodium (2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid (as per EP) ; Sodium (O-(4-hydroxy-3-iodophenyl)-3,5-diiodo-) L-Tyrosine) (as per USP)

Sinônimo: Liothyronine Sodium (USP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: IC1=CC(C[C@H](N)C([O-])=O)=CC(I)=C1OC2=CC=C(O)C(I)=C2.[Na+]

Levothyroxine EP Impurity A is chemically Sodium (2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid (as per EP) ; Sodium (O-(4-hydroxy-3-iodophenyl)-3,5-diiodo-) L-Tyrosine) (as per USP). It is also known as Liothyronine Sodium (USP). Levothyroxine EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Levothyroxine EP Impurity A 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 Levothyroxine.

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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