Methylprednisolone EP Impurity J

N° de SZ CAT:	SZ-M037010
Número CAS	53-36-1
Mol.F.	C24H32O6
Peso Molecular	416.5
Status de Fatura	In Stock
Shipping Condition	Ambient Temperature

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Nome Químico: 11β,17-dihydroxy-6α-methyl-3,20-dioxopregna-1,4-dien-21-yl acetate; methylprednisolone acetate; methylprednisolone hydrogen succinate EP impurity C

Sinônimo: Methylprednisolone Acetate (USP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: CC(OCC([C@@]1(O)CC[C@@]2([H])[C@]3([H])C[C@H](C)C4=CC(C=C[C@]4(C)[C@@]3([H])[C@@H](O)C[C@]12C)=O)=O)=O

Methylprednisolone and its related substances in freeze-dried powders for injections
ljiljana solomun1, svetlana ibrić2, vlatka vajs3#, ivan vučković3# and zorica vujić
J. Serb. Chem. Soc. 75 (10) 1441–1452 (2010)

Purity evaluation of 6wmethylprednisolone acetate by HPLC
e. ciranni signoretti,* l. valvo, a.l. savella and g. cavina
Journal of Pharmaceutical & Biomedical Analysis Vol. 11, No. 7, pp. 587-593,1993

Methylprednisolone EP Impurity J is chemically 11β,17-dihydroxy-6α-methyl-3,20-dioxopregna-1,4-dien-21-yl acetate; methylprednisolone acetate; methylprednisolone hydrogen succinate EP impurity C. It is also known as Methylprednisolone Acetate (USP). Methylprednisolone EP Impurity J is supplied with detailed characterization data compliant with regulatory guideline. Methylprednisolone EP Impurity J 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 Methylprednisolone.

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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