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Hydrocortisone EP Impurity N

Hydrocortisone dimer; 11β,17,21-Trihydroxy-21-(11β,17,21-trihydroxy-3,20-dioxopregn-4-en-21-yl)pregn-4-ene-3,20-dione; 1,4-bis((10R,11S,13S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2,3-dihydroxybutane-1,4-dione;

Specifications:

CAS No.

Mol F.

: C42H58O10

Mol W.

: 722.9

Cat No.

: SA15223

Appearance

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Product Name

: Hydrocortisone EP Impurity N

CAS No.

Mol F.

: C42H58O10

Mol W.

: 722.9

Cat No.

: SA15223

Appearance

Synonyms

: Hydrocortisone dimer; 11β,17,21-Trihydroxy-21-(11β,17,21-trihydroxy-3,20-dioxopregn-4-en-21-yl)pregn-4-ene-3,20-dione; 1,4-bis((10R,11S,13S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2,3-dihydroxybutane-1,4-dione;

Related API

: Hydrocortisone

Hydrocortisone EP Impurity N product with CAS: NA is also known as Hydrocortisone dimer. This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. Hydrocortisone EP Impurity N is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Hydrocortisone and its related formulations. Moreover, Hydrocortisone dimer is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

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