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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Fludrocortisone, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Fludrocortisone impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Fludrocortisone-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Fludrocortisone Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fludrocortisone D6 Stable Isotopes CS-O-20080 127-31-1 (Unlabeled) Enquire
Fludrocortisone-d5 Stable Isotopes CS-O-06627 127-31-1(Unlabeled) In Stock


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fludrocortisone API Standards CS-O-03515 127-31-1 In Stock
Fludrocortisone acetate API Standards CS-T-54721 514-36-3 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
6-β Hydroxy Fludrocortisone Impurities CS-P-02334 806-36-0 Enquire