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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

Fluorometholone Degradation-I

● Under Development

Catalogue No.:	VE0023465
CAS No.:	N/A
Mol. Formula:	C22H28O4
Mol. Weight:	356.46 g/mol

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Additional information on Fluorometholone Degradation-I

Parent drug

Fluorometholone

IUPAC Name

(6S, 10S, 11S, 13S, 14S, 17R)-17-acetyl-11, 17-dihydroxy-6, 10, 13-trimethyl-6, 7, 10, 11, 12, 13, 14, 15, 16, 17-decahydro-3H-cyclopenta[a]phenanthren-3-one

Pharmacopoeial Synonyms

N/A

Other Synonyms

N/A

Smiles

O=C1C=C[C@@]2(C)C([C@@]([H])(C)CC3=C2[C@](O)([H])C[C@@]4(C)[C@@]3([H])CC[C@]4(O)C(C)=O)=C1

InChI

InChI=1S/C22H28O4/c1-12-9-15-16-6-8-22(26, 13(2)23)21(16, 4)11-18(25)19(15)20(3)7-5-14(24)10-17(12)20/h5, 7, 10, 12, 16, 18, 25-26H, 6, 8-9, 11H2, 1-4H3/t12-, 16-, 18-, 20-, 21-, 22-/m0/s1

Description

The Fluorometholone Degradation-I standard is a well-characterized compound that aligns with key regulatory guidelines | including USP | EMA | JP | and BP. It plays a crucial role in analytical method development | method validation (AMV) | and quality control (QC) processes | particularly in the manufacturing of Fluorometholone. This impurity standard is valuable for both Abbreviated New Drug Applications (ANDA) and New Drug Applications (NDA) | ensuring reliable and precise analytical outcomes. To further support research and development | it comes with a comprehensive Structure Elucidation Report (SER) | providing detailed insights for advanced analysis.