Levobunolol API is a synthetic, non-selective beta-adrenergic receptor antagonist (beta-blocker) belonging to the oxazolidine derivative class. It is the S-enantiomer of bunolol and possesses pharmacological activity at both β₁- and β₂-adrenergic receptors. Levobunolol reduces adrenergic stimulation and, in ophthalmic applications, lowers intraocular pressure primarily by reducing the production of aqueous humor.
Chemically, Levobunolol is identified as 5-[3-[(1S)-3-tert-butylamino-2-hydroxypropoxy]-2-methylphenyl]-2(3H)-furanone. It has the molecular formula C₁₇H₂₅NO₄, molecular weight approximately 291.39 g/mol, and CAS number 47141-42-4.
Levobunolol is particularly associated with ophthalmic pharmaceutical formulations used for the management of elevated intraocular pressure and conditions such as ocular hypertension and glaucoma. As a stereochemically defined beta-blocker, its identity and enantiomeric purity are important quality attributes for pharmaceutical manufacturing.
MEDIOCON INC supplies Levobunolol for applicable pharmaceutical manufacturing, ophthalmic formulation development, analytical research, quality-control testing and bulk API requirements, subject to product availability, applicable regulatory requirements and batch-specific documentation.
| Parameter | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Levobunolol API Manufacturer & Supplier in India | MEDIOCON INC (CAS 47141-42-4) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Levobunolol API Manufacturer & Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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