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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Clobetasone, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Clobetasone 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 Clobetasone-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.

Clobetasone Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clobetasone 17-Butyrate-d7 Stable Isotopes CS-T-99652 Not Available Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
CLOBETASONE API CS-O-06280 54063-32-0 In Stock
Clobetasone Butyrate API CS-L-00022 25122-57-0 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Clobetasone 17-Propionate Impurity CS-TB-00576 25122-56-9 In Stock
Clobetasone Butyrate EP Impurity G Impurity CS-O-53033 ---- Enquire
Clobetasone Butyrate Impurity F Impurity CS-EO-00071 25120-98-3 Enquire