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Dexamethasone EP Impurity G

21-O-Acetyl Dexamethasone; Betamethasone Acetate EP Impurity B; Dexamethasone Isonicotinate EP Impurity B; (11β,16α)-21-(Acetyloxy)-9-fluoro-11,17-dihydroxy-16-methyl-pregna-1,4-diene-3,20-dione; 9-Fluoro-11β,17,21-trihydroxy-16α-methyl-pregna-1,4-diene-3,20-dione 21-Acetate

Dexamethasone-EP-Impurity-G

Specifications:

CAS No.

: 1177-87-3

Mol F.

: C24H31FO6

Mol W.

: 434.5

Cat No.

: SA15520

Appearance

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Product Name

: Dexamethasone EP Impurity G

CAS No.

: 1177-87-3

Mol F.

: C24H31FO6

Mol W.

: 434.5

Cat No.

: SA15520

Appearance

Synonyms

: 21-O-Acetyl Dexamethasone; Betamethasone Acetate EP Impurity B; Dexamethasone Isonicotinate EP Impurity B; (11β,16α)-21-(Acetyloxy)-9-fluoro-11,17-dihydroxy-16-methyl-pregna-1,4-diene-3,20-dione; 9-Fluoro-11β,17,21-trihydroxy-16α-methyl-pregna-1,4-diene-3,20-dione 21-Acetate

Related API

: Dexamethasone

Order Dexamethasone EP Impurity G impurity standard with CAS: 1177-87-3 and speed up your Dexamethasone project. This product is also known as 21-O-Acetyl Dexamethasone; Betamethasone Acetate EP Impurity B and can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This compound is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Dexamethasone and its related formulations. Moreover, 21-O-Acetyl Dexamethasone 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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