Halobetasol Propionate

Halobetasol Propionate
( 66852-54-8 )

Nova International is a premier manufacturer and global exporter of high-purity Active Pharmaceutical Ingredients (APIs). We deliver world-class Halobetasol Propionate manufactured under strict WHO-GMP compliant standards. Known for exceptional chemical purity and stability, our API ensures superior formulation performance for topical corticosteroids targeting severe skin inflammation.

Halobetasol Propionate

Technical Specification

Product Halobetasol Propionate
CAS Number 66852-54-8
Molecular Formula C₂₅H₃₁ClF₂O₅
Molecular Weight 484.96 g/mol
Appearance White to off-white crystalline powder
Purity (HPLC) Minimum 98.0%
Melting Point 220°C to 225°C
Solubility Soluble in dichloromethane and chloroform; practically insoluble in water

Key Features of Halobetasol Propionate

Ultra-High Purity

Rigorously batch-tested to an HPLC purity of not less than 98.0%.

Potent Corticosteroids Class

Super-high potency topical corticosteroid for fast-acting dermatological applications.

Compliance Ready

Manufactured in state-of-the-art facilities aligned with global regulatory guidelines.

Exceptional Stability

Formulated for long shelf-life and robust physical stability in creams and ointments.

Precise Particle Size

Processed with controlled particle size distribution for smooth topical blend homogeneity.

Secure Export Packaging

Packed in USP-compliant sealed containers to preserve chemical integrity during export.

FAQs

It’s a potent high-efficacy active pharmaceutical ingredient designed for topical drugs, and particularly is used in high-potency creams, ointments and lotions of topical applications aimed at the treatment of psoriasis and inflammatory dermatosis.

Nova International provides a CoA, SDS/MSDS and complete batch-traceability document set with every shipment.

At controlled storing conditions in its original airtight sealed containers in cool, dry conditions and safe from light, the chemical potency and integrity of the Halobetasol Propionate API will be 36 months.

We utilize validated HPLC testing and strict inline process controls at every synthesis stage to consistently limit impurities, control particle size distribution, and guarantee a minimum purity level of 98.0%.

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