Fludrocortisone Acetate Working Standard (Secondary Reference Standard)
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Documentation

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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.

514-36-3Fludrocortisone Acetate Working Standard (Secondary Reference Standard)

● Under Development

Catalogue No.:VE0027465
CAS No.:514-36-3
Mol. Formula:C23H31FO6
Mol. Weight:422.50 g/mol

Additional information on CAS 514-36-3

Parent drug

Fludrocortisone Acetate / Fludrocortisone

IUPAC Name

9-fluoro-11β,17,21-trihydroxypregn-4-ene-3,20-dione 21-acetate

Pharmacopeial Synonyms

N/A

Synonyms

N/A

Smiles

O=C1CC[C@@]2(C)C(CC[C@]3([H])[C@]2(F)[C@@]([H])(O)C[C@@]4(C)[C@@]3([H])CC[C@@]4(C(COC(C)=O)=O)O)=C1

InChI

InChI=1S/C23H31FO6/c1-13(25)30-12-19(28)22(29)9-7-16-17-5-4-14-10-15(26)6-8-20(14,2)23(17,24)18(27)11-21(16,22)3/h10,16-18,27,29H,4-9,11-12H2,1-3H3/t16-,17-,18-,20-,21-,22-,23-/m0/s1

Description

Fludrocortisone Acetate Working Standard (Secondary Reference Standard), CAS 514-36-3, is a characterized research-grade material provided with a lot-specific certificate of analysis detailing identity, assay, purity and related substance profiles determined by HPLC, NMR and mass spectrometry. Supplied with documented traceability and recommended storage conditions to maintain stability, the material is intended solely for research and analytical method development and is not certified for use as a primary reference standard for GMP QC batch release or regulatory stability studies. Specifications, handling precautions and expiration information support reliable analytical calibration and method validation workflows while maintaining compliance with current laboratory quality practices.

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