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Description

Only compendial components as listed in the monograph are shown below

Contents

Analyte

CAS Number

Concentration

Unit

Additional information

Method

Methylprednisolone

[83-43-2]

17,21-Dihydroxy-6alpha-methylpregna-1,4-diene-3,11,20-trione

[91523-05-6]

Methylprednisolone Related Compound A (11-Keto Methylprednisolone)

11beta,17,21,21-Tetrahydroxy-6alpha-methylpregna-1,4-diene-3,20-dione

[n/a]

Methylprednisolone Related Compound B (Methylprednisolone acetal)

11beta-Hydroxy-6alpha-methylandrosta-1,4-diene-3,17-dione

[61919-52-6]

Methylprednisolone Related Compound C (17-Keto Methylprednisolone)

11beta,20-Dihydroxy-6alpha-methylpregna-1,4,17(20)-triene-3,21-dione

[1338549-02-2]

Methylprednisolone Related Compound D (Methylprednisolone glyoxal)

11beta-Hydroxy-6?-methyl-3-oxoandrosta-1,4-diene-17beta-carboxylic acid

[229019-44-7]

Methylprednisolone Related Compound E (Methylprednisolone acid)

11beta,17,21-Trihydroxy-6alpha-methylpregn-4-ene-3,20-dione

[1625-39-4]

Methylprednisolone Related Compound F (Dihydromethylprednisolone)

(6alpha)-17,21-Dihydroxy-6-methylpregna-1,4,9(11)-triene-3,20-dione

[93269-35-3]

Methylprednisolone Related Compound G (Anhydromethylprednisolone)

11beta,17,21-Trihydroxy-6beta-methylpregna-1,4-diene-3,20-dione

[18462-27-6]

Methylprednisolone Related Compound H (6-Epimethylprednisolone)

Methylprednisolone Impurity I (USP)

[n/a]

Miscellaneous

Certificate of Analysis (specimen)

Reference Material CoA specimen: for the current lot, please contact your customer service representative at info@labmix24.com

Product data sheet

View all available product details e.g. description, analytes/parameters, CAS Number, concentrations/values, sales unit/product format, method, source, transport information

Download CV

US Pharmacopeia Standards set a global benchmark, enabling efficient, reliable, and cost-effective development and quality control of pharmaceuticals.

Official USP Reference Standards are highly characterized physical specimens intended for quality control use when conducting assays and tests for medicines as described in the USP-NF. When you conduct tests and assays required by the USP-NF using the USP reference standards specified, the results can be considered conclusive.

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